Xu, Yong-Kai’s team published research in Dalton Transactions in 2021 | CAS: 523-27-3

9,10-Dibromoanthracene(cas: 523-27-3) is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.Related Products of 523-27-3

Xu, Yong-Kai; Meng, Mei-Mei; Xi, Ji-Ming; Wang, Li-Fei; Zhu, Rui; Liu, Xing-Gui; Zhang, Rui; Dong, Wei; Lu, Zhen-Zhong; Zheng, He-Gen; Huang, Wei published an article in 2021. The article was titled 《Mixed matrix membranes containing fluorescent coordination polymers for detecting Cr2O72- with high sensitivity, stability and recyclability》, and you may find the article in Dalton Transactions.Related Products of 523-27-3 The information in the text is summarized as follows:

Three coordination polymers (CPs) were synthesized by using CdII, fluorescent 9,10-di(4-pyridyl)anthracene (dpa), and cyclohexane-1,4-dicarboxylic acid (H2cda), and they are [Cd2(dpa)2(cda)Cl2]n (1), [Cd(dpa)2(cda)]n (2) and [Cd(dpa)(cda)(H2O)]n (3). Both 1 and 2 are fluorescent and contain nonporous layers. 3 is an isomer of 2 and contains a porous diamondoid network. Fluorescent mixed matrix membranes were prepared by dispersing the particles of 1 or 2 within the matrix of polymethyl methacrylate, and showed high sensitivity and selectivity for detecting Cr2O72- in water. Both stability and recyclability of the MMMs were remarkably higher than those of the CP powders. In the experiment, the researchers used many compounds, for example, 9,10-Dibromoanthracene(cas: 523-27-3Related Products of 523-27-3)

9,10-Dibromoanthracene(cas: 523-27-3) is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.Related Products of 523-27-3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Sun, Qing’s team published research in Environmental Research in 2021 | CAS: 523-27-3

9,10-Dibromoanthracene(cas: 523-27-3) is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.Formula: C14H8Br2

Sun, Qing; Lu, Feng-Hui; Ni, Hong-Gang published an article in 2021. The article was titled 《Microplastic-water partitioning of two states halogenated PAHs: Solute and sol》, and you may find the article in Environmental Research.Formula: C14H8Br2 The information in the text is summarized as follows:

The complex interactions of contaminants with microplastics significantly affect ecol. risk assessments. Studies of the sorption behavior of freely dissolved hydrophobic organic contaminants (HOCs) on microplastics are common. However, concentrations of HOCs in the actual aquatic environment sometimes exceed their water solubility A possible explanation is that a microplastic-sol-water three-phase medium (TPM) is formed in the actual water environment. Both states HOCs (in solute and sol) have the potential to migrate to particles suspended in water. To confirm this view, four kinds of microplastics and eight halogenated polycyclic aromatic hydrocarbons (HPAHs) were selected to examine the partitioning of HPAHs between microplastics and water (sol and solute). Both monolayer and multilayer coverage of HPAHs onto microplastics occurred, and chem. sorption dominated the pseudo-sorption mechanism. The microplastic-water partition ratios of HPAHs (0.12-0.74) were approx. four to five orders of magnitude lower than their corresponding KOW values, suggesting that mechanisms other than sorption were involved. Apparently, the sol HPAHs contributed almost identically large increments to both microplastics and water, and closed the gap. For microplastic-supported HPAHs, the contribution of the sol fraction was more than triple that of the dissolved fraction; the key influencing factor was the water solubility of HPAHs. In the experiment, the researchers used 9,10-Dibromoanthracene(cas: 523-27-3Formula: C14H8Br2)

9,10-Dibromoanthracene(cas: 523-27-3) is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.Formula: C14H8Br2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Taherinia, Zahra’s team published research in ChemistrySelect in 2019 | CAS: 6630-33-7

o-Bromobenzaldehyde(cas: 6630-33-7) is used in L-threonine aldolase-catalyzed enantio/diastereoselective aldol reactions.Safety of o-BromobenzaldehydeIt is also used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.

The author of 《Decorated Peptide Nanofibers with Cu Nanoparticles: An Efficient Catalyst for the Multicomponent Synthesis of Chromeno[2,3-d]pyrimidin-8-amines, Quinazolines and 2H-Indazoles》 were Taherinia, Zahra; Ghorbani-Choghamarani, Arash; Hajjami, Maryam. And the article was published in ChemistrySelect in 2019. Safety of o-Bromobenzaldehyde The author mentioned the following in the article:

An efficient, simple and green protocol was developed for the synthesis of 7,10-diaryl-7H-benzo[7,8]chromeno[2,3-d]pyrimidin-8-amines I (R1 = Ph, 2-ClC6H4, 4-HOC6H4, etc.), 2-R2-substituted indazoles (R2 = Ph, 4-MeC6H4, 2,4-Cl2C6H3, etc.) and 2-R3-substituted quinazolines (R3 = Ph, 4-MeOC6H4) in the presence of peptide nanofibers decorated with Cu nanoparticles. Peptide nanofiber was synthesized by self-assembly technique. The effect of succinic anhydride was evaluated in two conditions: (i) without adding succinic anhydride at pH 4, (ii) by adding succinic anhydride at pH 5. Synthesized peptide nanofiber was characterized by 1H, 13C, DEPT NMR spectroscopies (Distortionless enhancement by polarization transfer), CHNSO, SEM, fluorescence spectroscopy, UV/Vis, FTIR and transmission electron microscopy (TEM). The experimental process involved the reaction of o-Bromobenzaldehyde(cas: 6630-33-7Safety of o-Bromobenzaldehyde)

o-Bromobenzaldehyde(cas: 6630-33-7) is used in L-threonine aldolase-catalyzed enantio/diastereoselective aldol reactions.Safety of o-BromobenzaldehydeIt is also used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Nasrollahzadeh, Mahmoud’s team published research in ACS Omega in 2019 | CAS: 586-76-5

4-Bromobenzoic acid(cas: 586-76-5) has been used to study the metabolic fate of 2-,3-and 4-bromo benzoic acids in rat hepatocytes incubation using high temperature liquid chromatography. It was used in bromine-specific detection of the metabolites of 2-,3-and 4-bromobenzoic acid in the urine and bile of rats by inductively coupled plasma mass spectrometry.Electric Literature of C7H5BrO2

The author of 《Magnetic Lignosulfonate-Supported Pd Complex: Renewable Resource-Derived Catalyst for Aqueous Suzuki-Miyaura Reaction》 were Nasrollahzadeh, Mahmoud; Issaabadi, Zahra; Varma, Rajender S.. And the article was published in ACS Omega in 2019. Electric Literature of C7H5BrO2 The author mentioned the following in the article:

A novel strategy is described to prepare magnetic Pd nanocatalyst by conjugating lignin with Fe3O4 nanoparticles via activation of calcium lignosulfonate, followed by combination with Fe3O4 nanoparticles. Tethering 5-amino-1H-tetrazole to calcium lignosulfonate-magnetite hybrid through 3-chloropropyl triethoxysilane enabled coordination of Pd salt with Fe3O4-lignosulfonate@5-amino-1H-tetrazole. The underlying changes of the lignosulfonate are identified, and the structural morphol. of attained Fe3O4-lignosulfonate@5-amino-1H-tetrazole-Pd(II) (FLA-Pd) is characterized by Fourier transform IR, thermogravimetry DTA, energy-dispersive spectrometry, field-emission SEM, transmission electron microscopy, and vibrating sample magnetometer (VSM). The synthesized FLA-Pd displayed high activity for phosphine-free C(sp2)-C(sp2) coupling in water, and the catalyst could be reused for seven successive cycles.4-Bromobenzoic acid(cas: 586-76-5Electric Literature of C7H5BrO2) was used in this study.

4-Bromobenzoic acid(cas: 586-76-5) has been used to study the metabolic fate of 2-,3-and 4-bromo benzoic acids in rat hepatocytes incubation using high temperature liquid chromatography. It was used in bromine-specific detection of the metabolites of 2-,3-and 4-bromobenzoic acid in the urine and bile of rats by inductively coupled plasma mass spectrometry.Electric Literature of C7H5BrO2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Rengarasu, Rathikrishnan’s team published research in Synlett in 2019 | CAS: 1530-32-1

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. CatOnium ETPB is also used as catalysts in the synthesis of certain organic compounds.Application of 1530-32-1

The author of 《Synthesis of a C1-C12 Fragment of Gulmirecin B》 were Rengarasu, Rathikrishnan; Maier, Martin E.. And the article was published in Synlett in 2019. Application of 1530-32-1 The author mentioned the following in the article:

The synthesis of a C1-C14 fragment I of the macrolide antibiotic gulmirecin B through formation of the C7-C8 bond by addition of a vinyllithium intermediate to a C1-C7 aldehyde was investigated. This crucial coupling was successful with a vinyllithium reagent corresponding to a C8-C12 fragment. The C8-C12 vinyl bromide II was prepared from L-malic acid. The C1-C7 aldehyde III building block was synthesized from hex-5-enoic acid by using an Evans alkylation, a cross-metathesis, and an asym. dihydroxylation as key steps. In the experimental materials used by the author, we found Ethyltriphenylphosphonium bromide(cas: 1530-32-1Application of 1530-32-1)

Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. CatOnium ETPB is also used as catalysts in the synthesis of certain organic compounds.Application of 1530-32-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Pakiet, Marta’s team published research in Bioelectrochemistry in 2019 | CAS: 629-03-8

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Category: bromides-buliding-blocks

The author of 《Gemini surfactant as multifunctional corrosion and biocorrosion inhibitors for mild steel》 were Pakiet, Marta; Kowalczyk, Iwona; Leiva Garcia, Rafael; Moorcroft, Robert; Nichol, Tim; Smith, Thomas; Akid, Robert; Brycki, Bogumil. And the article was published in Bioelectrochemistry in 2019. Category: bromides-buliding-blocks The author mentioned the following in the article:

Biocorrosion is an important type of corrosion which leads to economic losses across oil and gas industries, due to increased monitoring, maintenance, and a reduction in platform availability. Ideally, a chem. compound engineered to mitigate against biocorrosion would possess both antimicrobial properties, as well as efficient corrosion inhibition. Gemini surfactants have shown efficacy in both of these properties, however there still remains a lack of electrochem. information regarding biocorrosion inhibition. The inhibition of corrosion and biocorrosion, by cationic gemini surfactants, of carbon steel was investigated. The results showed that the inhibition efficiency of the gemini surfactants was high (consistently >95%), even at low concentrations Gemini surfactants also showed strong antimicrobial activity, with a min. inhibitory concentration (0.018 mM). Corrosion inhibition was investigated by electrochem. impedance spectroscopy (EIS) and linear polarisation resistance (LPR), with biocorrosion experiments carried out in an anaerobic environment. Surface morphol. was analyzed using SEM (SEM). In the part of experimental materials, we found many familiar compounds, such as 1,6-Dibromohexane(cas: 629-03-8Category: bromides-buliding-blocks)

1,6-Dibromohexane(cas: 629-03-8) is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are: synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications; synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Bauer, Adriano’s team published research in Chemical Science in 2019 | CAS: 14660-52-7

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact.Category: bromides-buliding-blocks

The author of 《Chemoselective formal β-functionalization of substituted aliphatic amides enabled by a facile stereoselective oxidation event》 were Bauer, Adriano; Maulide, Nuno. And the article was published in Chemical Science in 2019. Category: bromides-buliding-blocks The author mentioned the following in the article:

A facile and stereoselective dehydrogenation event enabling the functionalization of aliphatic amides, e.g., 1-(indolin-1-yl)-2-methylpropan-1-one at different positions in a one-pot fashion has been described. Derivatives of relevant pharmaceuticals were formally functionalized in the β-position in late-stage manner. A single-step synthesis of incrustoporine from a simple precursor further showcases the potential utility of this approach. The experimental part of the paper was very detailed, including the reaction process of Ethyl 5-bromovalerate(cas: 14660-52-7Category: bromides-buliding-blocks)

Ethyl 5-bromovalerate(cas: 14660-52-7) belongs to bromides. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact.Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

de Orbe, M. Elena’s team published research in ACS Catalysis in 2019 | CAS: 13465-09-3

Indium(III) bromide(cas: 13465-09-3) is used as a catalyst to produce dithioacetals when unactivated alkynes react with thiols and fields such as optics and microelectronics that utilize semiconductor technology have wide uses for indium in high-performing solar cells.SDS of cas: 13465-09-3

In 2019,ACS Catalysis included an article by de Orbe, M. Elena; Zanini, Margherita; Quinonero, Ophelie; Echavarren, Antonio M.. SDS of cas: 13465-09-3. The article was titled 《Gold- or Indium-Catalyzed Cross-Coupling of Bromoalkynes with Allylsilanes through a Concealed Rearrangement》. The information in the text is summarized as follows:

The gold(I)-catalyzed reaction of bromoalkynes with allylsilanes gives 1,4-enynes in a formal cross-coupling reaction. Mechanistic studies revealed the involvement of gold(I) vinylidenes or vinylidenephenonium gold(I) cations depending on the substituent on the bromoalkyne. In the case of bromo arylalkynes, the vinylidenephenonium gold(I) cations lead to 1,4-enynes via a 1,2-aryl rearrangement. The same reactivity has been observed in the presence of InBr3. In the part of experimental materials, we found many familiar compounds, such as Indium(III) bromide(cas: 13465-09-3SDS of cas: 13465-09-3)

Indium(III) bromide(cas: 13465-09-3) is used as a catalyst to produce dithioacetals when unactivated alkynes react with thiols and fields such as optics and microelectronics that utilize semiconductor technology have wide uses for indium in high-performing solar cells.SDS of cas: 13465-09-3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Yeap, Guan-Yeow’s team published research in Liquid Crystals in 2018 | CAS: 17696-11-6

8-Bromooctanoic acid(cas: 17696-11-6) acid is used in the synthesis of 8-(N-Methyl-4,4′-bipyridinyl)- octanoic acid. 8-Mercaptooctanoic acid was prepared from 8-bromooctanoic acid.Application In Synthesis of 8-Bromooctanoic acid

In 2018,Yeap, Guan-Yeow; Ooi, Yew-Hong published 《λ-Shaped liquid crystal trimers with dual terminal cholesteryl moieties: synthesis and concomitant of N*, SmA and cholesteric glassy phases》.Liquid Crystals published the findings.Application In Synthesis of 8-Bromooctanoic acid The information in the text is summarized as follows:

Two homologous series of λ-shaped chiral liquid crystal trimers composed of a laterally substituted benzylidene-aniline as the central core armed by two cholesteryl ester moieties via odd-even alkyl spacer are synthesized (I; X = halo, Me, OH; n = 4-10). All the compounds are mesogenic exhibiting both chiral nematic (N*) and SmA phases except for trimers bearing long spacers (n = 9-10). A pronounced odd-even effect is observed on the phase transition temperatures and clearing enthalpies when the spacer length is varied in which the even-parity members show higher value. The widening of N* phase upon elongation of the alkyl spacer can be interpreted as a result of the destabilization of SmA phase. Full recrystallization from the cholesteric phase upon cooling is not observed for all the compounds bearing long spacer, especially oxydecanoyl spacer. Instead, the anisotropic fluid vitrified to form the cholesteric glassy state characteristic of polymer at low temperature This finding is also evident from the polarizing optical microscope whereby non-crystalline texture which resembles the Grandjean texture with various reflection colors is observed upon cooling to low temperature The effect of the lateral substituents on the liquid-crystalline behavior is also discussed. In the experiment, the researchers used 8-Bromooctanoic acid(cas: 17696-11-6Application In Synthesis of 8-Bromooctanoic acid)

8-Bromooctanoic acid(cas: 17696-11-6) acid is used in the synthesis of 8-(N-Methyl-4,4′-bipyridinyl)- octanoic acid. 8-Mercaptooctanoic acid was prepared from 8-bromooctanoic acid.Application In Synthesis of 8-Bromooctanoic acid

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Hu, Xiao-Qiang’s team published research in Chemical Science in 2018 | CAS: 76006-33-2

3-Bromo-2-methylbenzoic acid(cas: 76006-33-2) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Quality Control of 3-Bromo-2-methylbenzoic acid Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.

In 2018,Hu, Xiao-Qiang; Hu, Zhiyong; Trita, A. Stefania; Zhang, Guodong; Goossen, Lukas J. published 《Carboxylate-directed C-H allylation with allyl alcohols or ethers》.Chemical Science published the findings.Quality Control of 3-Bromo-2-methylbenzoic acid The information in the text is summarized as follows:

A [Ru(p-cymene)Cl2]2 catalyst activated allyl alcs. and ethers for the regioselective ortho-C-H allylation of aromatic and heteroaromatic carboxylates. The reaction was orthogonal to most C-H functionalizations with allyl alcs. in that allyl arenes rather than carbonyl compounds were obtained. A wide range of substrates were thus smoothly transformed to allylarenes at 50 ° in phosphate-buffered 2,2,2-trichloroethanol. The reaction concept combined the use of abundant reagents and directing groups in a sustainable, waste-minimized method for C-C bond formation. The results came from multiple reactions, including the reaction of 3-Bromo-2-methylbenzoic acid(cas: 76006-33-2Quality Control of 3-Bromo-2-methylbenzoic acid)

3-Bromo-2-methylbenzoic acid(cas: 76006-33-2) belongs to organobromine compounds.Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Quality Control of 3-Bromo-2-methylbenzoic acid Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary