Tag: M.W=150-200

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 4897-84-1, formula is C5H9BrO2, The most pervasive is the naturally produced bromomethane. SDS of cas: 4897-84-1

Risi, Caterina;Calamante, Massimo;Cini, Elena;Faltoni, Valentina;Petricci, Elena;Rosati, Filippo;Taddei, Maurizio research published 《 In water alkylation of amines with alcohols through a borrowing hydrogen process catalysed by ruthenium nanoparticles》, the research content is summarized as follows. A simple and environmentally benign procedure for the synthesis of secondary amines in water has been developed. Combining Ru₃(CO)₁₂, tetraphenylcyclopentadienone and a small quantity of TGPS-750-M surfactant, primary and secondary alcs. were alkylated at N employing equimolar amounts of aromatic amines in water. The reaction occurs under microwave (MW) dielec. heating with high conversion and high yield. When required, the use of biomass-derived 2-MeTHF or GVL as a co-solvent is possible. Under the influence of MWs, a Ru nanoparticle-nanomicelle combination was formed acting as an effective and recyclable catalyst. This protocol was also employed for “in water” cyclization to synthesize biol. relevant pyrrolobenzodiazepines (PBDs).

SDS of cas: 4897-84-1, Methyl 4-bromobutyrate,also as known as 4-Bromobutyric acid methyl ester, is a useful research compound. Its molecular formula is C5H9BrO2 and its molecular weight is 181.03 g/mol. The purity is usually 95%.
4-Bromobutyric acid methyl ester is a synthetic compound that can be used to inhibit the activity of the G1 phase cyclin-dependent kinases. It has been shown to inhibit protein synthesis by alkylating the amino groups of proteins and fatty acids. 4-Bromobutyric acid methyl ester also inhibits the growth of cancer cell lines, such as renal carcinoma cells. The mechanism of action for this drug is not well understood, but it may be due to its ability to bind with monoclonal antibodies and enter kidney cells by passive diffusion., 4897-84-1.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 4897-84-1, formula is C5H9BrO2, Name is Methyl 4-bromobutanoate. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Application of C5H9BrO2.

Roberts, Brett L.;Ma, Zhi-Xiong;Gao, Ang;Leisten, Eric D.;Yin, Dan;Xu, Wei;Tang, Weiping research published 《 Two-Stage Strategy for Development of Proteolysis Targeting Chimeras and its Application for Estrogen Receptor Degraders》, the research content is summarized as follows. Proteolysis targeting chimeras (PROTACs) have emerged as useful chem. probes and potential therapeutics by taking advantage of the ubiquitin-proteasome system to degrade intracellular disease-associated proteins. PROTACs are heterobifunctional mols. composed of a target protein ligand, E3 ubiquitin ligase ligand, and a linker between them. The generation of efficient PROTACs requires screening of many parameters, especially the lengths and types of the linkers. The authors report the proof-of-concept study using a two-stage strategy to facilitate the development of PROTACs against the estrogen receptor (ER). In stage one, a library of close to 100 PROTACs was synthesized by simply mixing a library of ERα ligands containing a hydrazide functional group at different positions with a preassembled library of E3 ligase ligands bearing different types and lengths of linkers with a terminal aldehyde group in a 1:1 ratio. Cell-based screening occurred without further purification, because the formation of the acylhydrazone linkage is highly efficient and produces water as the only byproduct. Compound A3 was the most potent ER degrader in two ER+ cell lines (DC₅₀= ~10 nM, D_max= ≥ 95%). Stage two involved transformation to a more stable amide linker to generate a more drug-like mol. The new compound, AM-A3, showed comparable biol. activity (DC₅₀ = 1.1 nM, D_max = 98%) and induced potent antiproliferation (IC₅₀= 13.2 nM, I_max= 69%) in MCF-7. This proof-of -concept study demonstrates that the two-stage strategy can significantly facilitate the development of PROTACs against ER without the tedious process of making large numbers of PROTACs one by one. It has the potential to be expanded to many other targets.

4897-84-1, Methyl 4-bromobutyrate,also as known as 4-Bromobutyric acid methyl ester, is a useful research compound. Its molecular formula is C5H9BrO2 and its molecular weight is 181.03 g/mol. The purity is usually 95%.
4-Bromobutyric acid methyl ester is a synthetic compound that can be used to inhibit the activity of the G1 phase cyclin-dependent kinases. It has been shown to inhibit protein synthesis by alkylating the amino groups of proteins and fatty acids. 4-Bromobutyric acid methyl ester also inhibits the growth of cancer cell lines, such as renal carcinoma cells. The mechanism of action for this drug is not well understood, but it may be due to its ability to bind with monoclonal antibodies and enter kidney cells by passive diffusion., Application of C5H9BrO2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 4224-70-8, formula is C6H11BrO2, Name is 6-Bromohexanoic acid. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Electric Literature of 4224-70-8.

Roemer, Max;Goncales, Vinicius R.;Keaveney, Sinead T.;Pernik, Indrek;Lian, Jiaxin;Downes, James;Gooding, J. Justin;Messerle, Barbara A. research published 《 Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes》, the research content is summarized as follows. A series of Rh- and Ir-hybrid catalysts with varying tether lengths has been prepared by immobilization of Rh^I, Rh^III and Ir^III complexes on carbon black via radical grafting. The performance of the different catalysts was assessed for the hydrosilylation of phenylacetylene with Et₃SiH. The efficiency of the catalysts was dependent on the length of the tethers to the surface. The Rh^III– and Ir^III hybrids afforded the β(Z)-vinylsilanes, as observed for the analogous homogeneous Rh^III catalyst. No distinct product selectivity was observed when using the homogeneous Rh^I precursors as catalysts. However, on using the Rh^III hybrid catalysts derived from the Rh^I precursors to promote hydrosilylation, the major products were the α-vinylsilanes and the origin of the difference in reactivity was found to be a chem. modification of the catalysts during immobilization. Substrate scope is demonstrated for a number of alkynes, and feasible mechanisms supported by DFT calculations are proposed.

Electric Literature of 4224-70-8, 6-bromohexanoic acid is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. It derives from a hexanoic acid.
6-Bromohexanoic acid is a useful research compound. Its molecular formula is C6H11BrO2 and its molecular weight is 195.05 g/mol. The purity is usually 95%.
6-Bromohexanoic acid is useful for the preparation of anti-CTLA4 compounds as antitumor agents.
6-Bromohexanoic acid is a fatty acid that has been shown to be an effective agent for the treatment of cancer. It is used in gene therapy to inhibit the growth of cancer cells by binding to and then activating transcription factors. 6-Bromohexanoic acid can also be used as a chemotherapeutic agent and has been shown to cause apoptosis in monoclonal antibody-treated cells. 6-Bromohexanoic acid has pharmacokinetic properties that are similar to those of other fatty acids. The reaction solution was found to have high chemical stability, which may be due to the presence of nitrogen atoms. This reaction solution was found to adsorb onto the surface of monoclonal antibodies and cell culture, altering their properties., 4224-70-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine. 70-23-5, formula is C5H7BrO3, Name is Ethyl 3-bromo-2-oxopropanoate, HPLC of Formula: 70-23-5

Rostamian, Rezvaneh;Khalilzadeh, Mohammad A.;Zareyee, Daryoush research published 《 Wood ash biocatalyst as a novel green catalyst and its application for the synthesis of benzochromene derivatives》, the research content is summarized as follows. This study investigates the catalytic activity of wood ash as a heterogeneous catalyst for the synthesis of benzochromene derivatives I (R = Me, 4-methoxyphenyl, Ph, Et, 4-methylphenyl; R₁ = 4-methoxyphenyl, C(O)OC₂H₅, 4-methylphenyl). Several wood ash catalysts, comprising calcium- and potassium-rich carbonates, were prepared from different natural resources under various combustion temperatures The prepared catalysts were characterized by Fourier transform IR, SEM, energy dispersive X-ray anal., transmission electron microscopy, and X-ray diffraction techniques. Catalytic efficiency of the resultant catalysts was tested in the synthesis of benzochromene derivatives I. The exptl. studies clarified that the catalyst prepared at 850°C could efficiently expedite the formation of three-component synthesis of benzochromene derivatives I in water at 80°C with high yields. Indeed, alkali, alk. metal, and metal oxides such as Al₂O₃, SiO₂, MgO, CaO, and Fe₂O₃, are widely utilized as both catalyst and catalyst support in the heterogeneous catalytic processes. The prepared wood ash catalysts (possessing metal oxides, e.g., CuO, Al₂O₃, SiO₂, and CaO) could effectively prompt the electrophilic activity of the carbonyl groups during the nucleophilic attack intermediate, enhancing the efficiency of the reactions.

70-23-5, Ethyl bromopyruvate molecular formula is C5H7BrO3 and its molecular weight is 195.01 g/mol. The purity is usually 95%.

Ethyl bromopyruvate is used in a synthesis of thioxothiazolidines from carbon disulfide and primary amines.

Ethyl bromopyruvate is a chemical inhibitor that inhibits the enzyme pyruvate dehydrogenase, which is responsible for the conversion of pyruvic acid to acetyl-CoA. This inhibition leads to a decrease in ATP levels and can cause metabolic disorders. Ethyl bromopyruvate is used as an anthelmintic drug and in asymmetric synthesis. It is also used in the synthesis of thiostrepton, an antibiotic that has been shown to have antimicrobial activity against Gram-positive bacteria, including Staphylococcus aureus and Streptococcus pneumoniae., HPLC of Formula: 70-23-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 4224-70-8, formula is C6H11BrO2, Name is 6-Bromohexanoic acid. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Synthetic Route of 4224-70-8.

Ruffell, Katie;Smith, Frances R.;Green, Michael T.;Nicolle, Simon M.;Inman, Martyn;Lewis, William;Hayes, Christopher J.;Moody, Christopher J. research published 《 Diazophosphonates: Effective Surrogates for Diazoalkanes in Pyrazole Synthesis》, the research content is summarized as follows. Diazophosphonates, readily prepared from α-ketophosphonates by oxidation of the corresponding hydrazones in batch or in flow, are useful partners in 1,3-dipolar cycloaddition reactions to alkynes to give N-H pyrazoles, including the first intramol. examples of such a process. The phosphoryl group imbues a number of desirable properties into the diazo 1,3-dipole. The electron-withdrawing nature of the phosphoryl stabilizes the diazo compound making it easier to handle, while the ability of the phosphoryl group to migrate readily in a [1,5]-sigmatropic rearrangement enables its transfer from C to N to aromatize the initial cycloadduct, and hence its facile removal from the final pyrazole product. Overall, the diazophosphonate acts as a surrogate for the much less stable diazoalkane in cycloadditions, with the phosphoryl group playing a vital, but traceless, role. The cycloaddition proceeds more readily with alkynes bearing electron-withdrawing groups, and is regiospecific with asym. alkynes. The potential of diazophosphonates for use in bioorthogonal cycloadditions is demonstrated by their facile addition to strained alkynes.

4224-70-8, 6-bromohexanoic acid is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. It derives from a hexanoic acid.
6-Bromohexanoic acid is a useful research compound. Its molecular formula is C6H11BrO2 and its molecular weight is 195.05 g/mol. The purity is usually 95%.
6-Bromohexanoic acid is useful for the preparation of anti-CTLA4 compounds as antitumor agents.
6-Bromohexanoic acid is a fatty acid that has been shown to be an effective agent for the treatment of cancer. It is used in gene therapy to inhibit the growth of cancer cells by binding to and then activating transcription factors. 6-Bromohexanoic acid can also be used as a chemotherapeutic agent and has been shown to cause apoptosis in monoclonal antibody-treated cells. 6-Bromohexanoic acid has pharmacokinetic properties that are similar to those of other fatty acids. The reaction solution was found to have high chemical stability, which may be due to the presence of nitrogen atoms. This reaction solution was found to adsorb onto the surface of monoclonal antibodies and cell culture, altering their properties., Synthetic Route of 4224-70-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 629-04-9, formula is C7H15Br, The most pervasive is the naturally produced bromomethane. SDS of cas: 629-04-9

Russell, Richard W.;Barker, Timothy J. research published 《 Transition Metal-Free sp³-sp³ Carbon-Carbon Coupling between Benzylboronic Esters and Alkyl Bromides》, the research content is summarized as follows. A transition metal-free coupling reaction of benzylboronic esters and alkyl halides to form compounds PhCH₂R [R = CH₂(CH₂)₅CH₃, CH₂(CH₂)₂CH=CH₂, CH₂(CH₂)₃CH₂OTIPS, etc.] was developed. Both alkyl bromides and alkyl iodides were found to be competent substrates with the nucleophilic boronate intermediate generated from the combination of benzylboronic ester and an alkyllithium. Good chemoselectivity was observed for the reaction with the alkyl bromide in substrates with a second electrophile present. Both secondary and tertiary benzylboronic esters were effective nucleophiles in the reaction with primary alkyl halides. Mechanistic observations were consistent with a radical mechanism.

SDS of cas: 629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Formula: C7H15Br.

Ryu, Jiwon;Manivannan, Ramalingam;Son, Young-A. research published 《 Azo dye-based optical probe for the detection toward mimic molecule of date rape drug》, the research content is summarized as follows. The azo dye-based visual responsive optical probe 5-(diheptylamino)-2-((3,5-dinitrothiophen-2-yl)diazenyl)phenol (DP), for the purpose of detection toward the mimic mol. of date rape drug was designed, synthesized and characterized. The recognizing abilities toward the mimic mol. (sodium butyrate) of date rape drug (gamma-hydroxybutyric acid) were examined in water. The prepared mol. was visually, anal., and theor. confirmed with the sensing ability of the probe. Developing an easy-to-use sensor kit will work spontaneously with a detectable colorimetric response in daylight. Obtained color change from light turquoise color to bluish-purple toward sodium butyrate containing alc. beverages was successfully recognized and confirmed. Even though the color change from light turquoise to bluish-purple obtained, which is not easily recognized clearly with the eye under normal light, UV-Visible spectra indicate the changes, thus the probe can be utilized productively to protect the victim from sexual assault.

Formula: C7H15Br, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 6911-87-1, formula is C7H8BrN, The most pervasive is the naturally produced bromomethane. Quality Control of 6911-87-1

Saadati, Fariba;Griffin, Samuel E.;Schafer, Laurel L. research published 《 Guanidinate Early-Transition-Metal Complexes: Efficient and Selective Hydroaminoalkylation of Alkenes》, the research content is summarized as follows. The influence of N,N-chelating guanidinate ligands on the reactivity of in situ generated Ta complexes for the intermol. hydroaminoalkylation of amines were explored. Increased conversion was observed with the Na salt of 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBDNa) paired with the Ta precursor Ta(CH₂SiMe₃)₃Cl₂ at 110°. Terminal alkenes underwent hydroaminoalkylation with a variety of secondary amine substrates to give substituted secondary amine products. Mono- and bis(guanidinate) Ta complexes were prepared, and their structures were studied. Importantly, the guanidinate ligand could be alkylated in the β position using Ta(NMe₂)₅ as a precatalyst to give the linear regioisomer as the major product, and this substituted ligand gave improved hydroaminoalkylation conversion in comparison to the parent ligand.

6911-87-1, 4-Bromo-N-methylaniline is a aniline based compound known to exhibit mutagenic properties.
4-Bromo-N-methylaniline is a useful research compound. Its molecular formula is C7H8BrN and its molecular weight is 186.05 g/mol. The purity is usually 95%.
4-Bromophenylmethylamine is an organic compound that has anti-inflammatory properties and is used as a pharmaceutical. It belongs to the group of amines. The hydrolysis of 4-bromophenylmethylamine by hydrochloric acid produces phenol and bromamine (NHBr). The reaction system can be used to synthesize a number of compounds, including anilines, benzofurans, and other aromatic compounds. 4-Bromophenylmethylamine reacts with muscle tissue in a similar manner as acetaminophen does. This drug also has been shown to have significant effects on the energy metabolism in the muscles of rats that are given carbon source., Quality Control of 6911-87-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 70-23-5, formula is C5H7BrO3, The most pervasive is the naturally produced bromomethane. COA of Formula: C5H7BrO3

Sadeghi Meresht, Abdollah;Ezzatzadeh, Elham;Dehbandi, Behnam;Salimifard, Masoomeh;Rostamian, Rezvaneh research published 《 Fe₃O₄/CuO Nanocomposite Promoted Green Synthesis of Functionalized Quinazolines Using Water Extract of Lettuce Leaves as Green Media: Study of Antioxidant Activity》, the research content is summarized as follows. In this work, five component reactions are utilized for the production of quinazoline derivatives by utilizing the one-pot reaction of 3-hydroxyphthalaldehyde, ethylenediamine, alkyl bromides, electron deficient acetylenic compounds and Et bromoacetate in vicinity of Fe₃O₄/CuO nanocomposites as a high performance catalyst at environment temperature in water extract of lettuce leaves as green solvent. Also, water extract of lettuce leaves was used for synthesis of Fe₃O₄/CuO nanocomposites. The existing quinazoline core in the synthesized compounds caused to ability of antioxidation of synthesized quinazoline. For confirmation of this point, we are used DPPH radical trapping and ferric ion reducing power tests. Outcomes of these tests show that synthesized quinazolines have low DPPH radical trapping and good reducing ability of ferric ion. The excellent yield of reaction, green media and easy separation of product and catalyst are some benefits of this procedure. Highlights water extract of Lettuce leaves was used as solvent for the preparation of quinazolines as cyclic heteroaromatic systems. The present procedure avoids the use of toxic solvent. The present procedure runs in water extract of Lettuce leaves as a green media. This recoverable catalyst makes this protocol attractive and useful as an industrially viable and eco-safe solvent with high yields of products.

COA of Formula: C5H7BrO3, Ethyl bromopyruvate molecular formula is C5H7BrO3 and its molecular weight is 195.01 g/mol. The purity is usually 95%.

Ethyl bromopyruvate is used in a synthesis of thioxothiazolidines from carbon disulfide and primary amines.

Ethyl bromopyruvate is a chemical inhibitor that inhibits the enzyme pyruvate dehydrogenase, which is responsible for the conversion of pyruvic acid to acetyl-CoA. This inhibition leads to a decrease in ATP levels and can cause metabolic disorders. Ethyl bromopyruvate is used as an anthelmintic drug and in asymmetric synthesis. It is also used in the synthesis of thiostrepton, an antibiotic that has been shown to have antimicrobial activity against Gram-positive bacteria, including Staphylococcus aureus and Streptococcus pneumoniae., 70-23-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. COA of Formula: C7H15Br.

Safari, Niloufar;Shirini, Farhad;Tajik, Hassan;Saielli, Giacomo research published 《 NMR and DFT studies of the aggregation behavior of dicationic dialkyl DABCO bistriflimide salts in solution》, the research content is summarized as follows. In this study, various derivatives of 1,4-dialkyl-diazabicyclo[2.2.2]octane-1,4-diium bis(trifluoromethanesulfonyl)imide salts, [C_n.DABCO.C_n][Tf₂N]₂, with different alkyl groups, were synthesized and characterized by their m.ps. and NMR spectra. Moreover, various solutions of [C₄.DABCO.C₄][Tf₂N]₂ and [C₈.DABCO.C₈][Tf₂N]₂ salts in deuterated methanol and acetone in different concentrations were prepared The effect of solvent polarity, concentration and charge d. of the cation on the aggregation behavior of these salts were investigated using ESI-mass spectrometry, ¹H NMR, DOSY NMR experiments and DFT calculations The obtained results showed that in methanol, a protic and very polar solvent, the chem. shift of DABCO protons and the diffusion coefficient of the cation are almost independent of the concentration, except for relatively high concentrations Thus, in this solvent and in the low concentration regime, aggregation is not favored and in high concentration small aggregates can be formed. In contrast, when dissolved in acetone, a less polar solvent, aggregates formation is favored. As a result, chem. shift of DABCO protons and diffusion coefficient of the cation in acetone are more strongly dependent on the concentration

629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., COA of Formula: C7H15Br

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary