Category: 629-04-9

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. Electric Literature of 629-04-9.

Shanker, G.;Srinatha, M. K.;Sandhya Kumari, D.;Ranjitha, B. S.;Alaasar, M. research published 《 Novel green synthetic approach for liquid crystalline materials using multi-component reactions》, the research content is summarized as follows. Synthesis of disk-shape liquid crystalline materials using multi-component reactions is reported. Two new series, the compounds I (R = n-C_nH_2n+1; n = 6, 7, 8, 10, 11, 12) and II, were synthesized by coupling either 2,3-dihydroxynaphthalene or 2,6-dihydroxynaphthalene with the corresponding 3,4,5-tris(alkoxy)anilines under solvent-free conditions. The mol. structures of the new materials were confirmed using ¹H NMR, ¹³C NMR and CHN elemental anal. The phase behavior was investigated using polarizing optical microscope and differential scanning calorimetry experiments All the materials exhibited room temperature discotic nematic phase during the cooling cycles as confirmed by X-ray diffraction studies. This synthetic approach provides multiple advantages such as high atom economy, short reaction time, mild reaction condition, simple workup, and do not require column chromatog. purification

Electric Literature of 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. Synthetic Route of 629-04-9.

Sharma, Neha;Gupta, Monika;Chowhan, Bushra;Frontera, Antonio research published 《 Magnetically separable nanocatalyst (IL@CuFe₂O₄-L-Tyr-TiO₂/TiTCIL): Preparation, characterization and its applications in 1,2,3-triazole synthesis and in photodegradation of MB》, the research content is summarized as follows. The present work encompasses the synthesis of novel heterogeneous magnetic nanocatalyst(IL@CuFe₂O₄-L-Tyr-TiO₂/TiTCIL) and its characterization by Fourier-transform IR spectroscopy (FTIR), high-resolution transmission electron microscopy (HR-TEM), field emission gun SEM (FEG-SEM), energy-dispersive X-ray spectroscopy (EDX), vibrating sample magnetometry (VSM), X-ray powder diffraction (P-XRD), XPS, photoluminescence spectroscopy and Raman spectroscopy. XPS anal. confirms the presence of Cu as Cu¹⁺ and Cu²⁺ by the effect of the linker in IL@CuFe₂O₄-L-Tyr-TiO₂/TiTCIL. It provides an eco-friendly procedure with several advantages such as operational simplicity, water as the solvent, short reaction time, easy workup and excellent yields in the synthesis of 1,4-disubstituted-1,2,3-triazoles via Click reaction. The catalyst showed recyclability up to seven runs in Click reaction and the recycled catalyst was also characterized by HR-TEM, FEG-SEM and XPS. In Click reaction, one single crystal of 1-benzyl-4-phenyl-1H-1,2,3-triazole was grown. Its energetic features, non-covalent interactions, mol. electrostatic potential surfaces, and packing arrangement were calculated by using the B3LYP-D3/def2-TZVP level of theory and the Bader’s quantum theory of “Atoms in mols.” (QTAIM). Moreover, IL@CuFe₂O₄-L-Tyr-TiO₂/TiTCIL also displayed good photocatalytic activity in the degradation of methylene blue dye in visible light.

Synthetic Route of 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

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Organic compounds having carbon bonded to bromine are called organic bromides. HPLC of Formula: 629-04-9.

Sheng, Jie;Ni, Hui-Qi;Ni, Shan-Xiu;He, Yan;Cui, Ru;Liao, Guang-Xu;Bian, Kang-Jie;Wu, Bing-Bing;Wang, Xi-Sheng research published 《 Diversity-Oriented Synthesis of Aliphatic Fluorides via Reductive C(sp³)-C(sp³) Cross-Coupling Fluoroalkylation》, the research content is summarized as follows. A direct nickel-catalyzed monofluoromethylation of unactivated alkyl halides e.g., (3-bromopropyl)benzene using a low-cost industrial raw material, bromofluoromethane, by demonstrating a general and efficient reductive cross-coupling of two alkyl halides e.g., (3-bromopropyl)benzene and e.g., (2-bromo-2-fluoroethyl)benzene was described. Results with 1-bromo-1-fluoroalkane also demonstrate the viability of monofluoroalkylation, which further established the first example of reductive C(sp³)-C(sp³) cross-coupling fluoroalkylation. These transformations demonstrate high efficiency, mild conditions, and excellent functional-group compatibility, especially for a range of pharmaceuticals and biol. active compounds Mechanistic studies support a radical pathway. Kinetic studies reveal that the reaction is first-order dependent on catalyst and alkyl bromide whereas the generation of monofluoroalkyl radical is not involved in the rate-determining step. This strategy provides a general and efficient method for the synthesis of aliphatic fluorides e.g, (4-fluorobutyl)benzene.

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., HPLC of Formula: 629-04-9

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. Computed Properties of 629-04-9

Shah, Priyanka;Soni, Rina;Soman, Shubhangi S. research published 《 Synthesis and mesomorphic properties of bis ester derivatives of coumarin containing chalcone linkage》, the research content is summarized as follows. Bis ester derivatives of coumarin containing chalcone linkage with various terminal alkoxy groups were designed, synthesized and characterized. Compounds 11a-m were studied for their mesomorphic properties using polarizing optical microscope and differential scanning calorimetry and photophys. properties using UV-vis and fluorescence spectroscopy. In this particular homologous series, compounds having lower flexible alkoxy chains showed very good mesogenic property with nematic mesophase formation, while analogs with higher chains failed to show any liquid crystalline property. Compound 11a with methoxy group showed very good absorbance and fluorescence as compared to higher chain length analogs.

Computed Properties of 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 compounds having carbon bonded to bromine are called organic bromides. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Product Details of C7H15Br.

Sargazi, Saman;Shahraki, Sheida;Shahraki, Omolbanin;Zargari, Farshid;Sheervalilou, Roghayeh;Maghsoudi, Saeid;Soltani Rad, Mohammad Navid;Saravani, Ramin research published 《 8-Alkylmercaptocaffeine derivatives: antioxidant, molecular docking, and in-vitro cytotoxicity studies》, the research content is summarized as follows. Due to their unique pharmacol. characteristics, methylxanthines are known as therapeutic agents in a fascinating range of medicinal scopes. In this report, we aimed to examine some biol. effects of previously synthesized 8-alkylmercaptocaffeine derivatives Cytotoxic and antioxidative activity of 8-alkylmercaptocaffeine derivatives were measured in malignant A549, MCF7, and C152 cell lines. Assessment of cGMP levels and caspase-3 activity were carried out using a colorimetric competitive ELISA kit. Computational approaches were employed to discover the inhibitory mechanism of synthesized compounds Among the twelve synthesized derivatives, three compounds (C1, C5, and C7) bearing Pr, heptyl, and 3-methyl-Bu moieties showed higher and more desirable cytotoxic activity against all the studied cell lines (IC₅₀ < 100μM). Furthermore, C5 synergistically enhanced cisplatin-induced cytotoxicity in MCF-7 cells (CI < 1). Both C5 and C7 significantly increased caspase-3 activity and intracellular cGMP levels at specific time intervals in all studied cell lines (P < 0.05). However, these derivatives did not elevate LDH leakage (P > 0.05) and exhibited no marked ameliorating effects on oxidative damage (P > 0.05). Computational studies showed that H-bond formation between the nitrogen atom in pyrazolo[4,3-D] pyrimidine moiety with Gln817 and creating a hydrophobic cavity result in the stability of the alkyl group in the PDE5A active site. We found that synthesized 8-alkylmercaptocaffeine derivatives induced cell death in different cancer cells through the cGMP pathway. These findings will help us to get a deeper insight into the role of methylxanthines as useful alternatives to conventional cancer therapeutics.

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., Product Details of C7H15Br

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

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

Organic compounds having carbon bonded to bromine are called organic bromides. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Application In Synthesis of 629-04-9.

Qi, Liangliang;Pang, Xiaobo;Yin, Kai;Pan, Qiu-Quan;Wei, Xiao-Xue;Shu, Xing-Zhong research published 《 Mn-mediated reductive C(sp³)-Si coupling of activated secondary alkyl bromides with chlorosilanes》, the research content is summarized as follows. Reductive coupling of activated secondary alkyl halides FG-CHXR¹ (FG = phosphinyl, sulfonyl; R¹ = Me, Et, PhCH₂CH₂, C₆H₁₃) with chlorosilane ClSiMe₂(CH:CH₂) mediated by manganese metal afforded secondary alkylsilanes FG-CH(R¹)SiMe₂(CH:CH₂) with high yields. The construction of secondary alkylsilanes is a challenging subject in the synthetic community. The cross-coupling provides a practical solution to address this problem, but it typically relies on organometallic species. Herein, we report an Mn-mediated reductive C(sp³)-Si coupling to synthesize these compounds from alkyl and silyl electrophiles. This approach avoids the requirement for activation of Si-Cl by transition metals and thus allows for the coupling of various common chlorosilanes. The reaction proceeds under mild conditions and shows good functional group compatibility. The method offers access to α-silylated organophosphorus and sulfones with a scope that is complementary to those obtained from the established methods.

Application In Synthesis of 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

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. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane, Recommanded Product: 1-Bromoheptane

Qiu, Xinkai;Rousseva, Sylvia;Ye, Gang;Hummelen, Jan C.;Chiechi, Ryan C. research published 《 In Operando Modulation of Rectification in Molecular Tunneling Junctions Comprising Reconfigurable Molecular Self-Assemblies》, the research content is summarized as follows. The reconfiguration of mol. tunneling junctions during operation via the self-assembly of bilayers of glycol ethers is described. Well-established functional groups are used to modulate the magnitude and direction of rectification in assembled tunneling junctions by exposing them to solutions containing different glycol ethers. Variable-temperature measurements confirm that rectification occurs by the expected bias-dependent tunneling-hopping mechanism for these functional groups and that glycol ethers, besides being an unusually efficient tunneling medium, behave similarly to alkanes. Memory bits are fabricated from crossbar junctions prepared by injecting eutectic Ga-In (EGaIn) into microfluidic channels. The states of two 8-bit registers were set by trains of droplets such that they are able to perform logical AND operations on bit strings encoded into chem. packets that alter the composition of the crossbar junctions through self-assembly to effect memristor-like properties. This proof-of-concept work demonstrates the potential for fieldable devices based on mol. tunneling junctions comprising self-assembled monolayers and bilayers.

Recommanded Product: 1-Bromoheptane, 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