Yuan, Bing’s team published research in ACS Catalysis in 12 | CAS: 111-83-1

ACS Catalysis published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C7H11N, HPLC of Formula: 111-83-1.

Yuan, Bing published the artcileNickel-Catalyzed Regioselective Reductive Ring Opening of Aryl Cyclopropyl Ketones with Alkyl Bromides, HPLC of Formula: 111-83-1, the publication is ACS Catalysis (2022), 12(8), 4261-4267, database is CAplus.

Herein, the successful implementation of reductive strategy in the ring opening reaction of aryl cyclopropyl ketones with unactivated alkyl bromides was reported for the synthesis of ketones. Under the catalysis of nickel, this reductive Csp3-Csp3 cross-coupling reaction proceeds with complete regioselectivity and bypasses the use of pregenerated organometallics, enabling efficient synthesis of alkylated ketones with high step economy and functionality tolerance.

ACS Catalysis published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C7H11N, HPLC of Formula: 111-83-1.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Yuan, Jia-cheng’s team published research in Huaxue Shijie in 52 | CAS: 111865-47-5

Huaxue Shijie published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C12H20O6, Application In Synthesis of 111865-47-5.

Yuan, Jia-cheng published the artcileSynthesis of 2-bromo-4-methoxyaniline in ionic liquid, Application In Synthesis of 111865-47-5, the publication is Huaxue Shijie (2011), 52(12), 747-750, database is CAplus.

A method for synthesis of 2-bromo-4-methoxyaniline in ionic liquid was introduced. The title compound was prepared from p-methoxyaniline through bromination. The 2-bromo-4-methoxyaniline was obtained in 98.2% yield and 99.5% purity. The effect of various brominating agents and their amounts, reaction temperature and reaction time on the bromination reaction was investigated. The new procedure for preparing 2-bromo-4-methoxyaniline has the advantages of easy source of material, good yield, simple operation and environmental benignity. Ionic liquid can be reused.

Huaxue Shijie published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C12H20O6, Application In Synthesis of 111865-47-5.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Regueiro-Figueroa, Martin’s team published research in Inorganic Chemistry in 49 | CAS: 166821-88-1

Inorganic Chemistry published new progress about 166821-88-1. 166821-88-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Boronic acid and ester,Benzyl bromide,Benzene,Boronic Acids,Boronic acid and ester, name is 2-(2-(Bromomethyl)phenyl)-5,5-dimethyl-1,3,2-dioxaborinane, and the molecular formula is C12H16BBrO2, SDS of cas: 166821-88-1.

Regueiro-Figueroa, Martin published the artcileMolecular Recognition of Sialic Acid by Lanthanide(III) Complexes through Cooperative Two-Site Binding, SDS of cas: 166821-88-1, the publication is Inorganic Chemistry (2010), 49(9), 4212-4223, database is CAplus and MEDLINE.

Herein the authors report two new ligands, 1,4,7-tris(carboxymethyl)-10-[2-(dihydroxyboranyl)benzyl]-1,4,7,10-tetraazacyclododecane (L1) and 1,4,7-tris(carboxymethyl)-10-[3-(dihydroxyboranyl)benzyl]-1,4,7,10-tetraazacyclododecane (L2), which contain a phenylboronic acid (PBA) function and a 1,4,7,10-tetraazacyclododecane-1,4,7-triacetate cage for complexation of lanthanide ions in an aqueous solution The pKa of the PBA function amounts to 4.6 in [Gd(L1)] and 8.9 in [Gd(L2)], with the value of the L2 analog being very similar to that of PBA (8.8). These results are explained by the coordination of the PBA function of L1 to the GdIII ion, which results in a dramatic lowering of its pKa. As a consequence, [Gd(L1)] does not bind to saccharides at physiol. pH. The nuclear magnetic relaxation dispersion profiles recorded for [Gd(L1)] and [Gd(L2)] confirm that the phenylboronate function is coordinated to the metal ion in the L1 derivative, which results in a q = 0 complex. The interaction of the [Gd(L2)] complex with 5-acetylneuraminic acid (Neu5Ac) and 2-α-O-methyl-5-acetylneuraminic acid (MeNeu5Ac) was studied by spectrophotometric titrations in an aqueous solution (pH 7.4, 0.1M 3-(N-morpholino)propanesulfonic acid buffer). Also, the authors have also studied the binding of these receptors with competing monosaccharides such as D-(+)-glucose, D-fructose, D-mannose, D-galactose, Me α-D-galactoside, and Me α-D-mannoside. The binding constants obtained indicate an important selectivity of [Gd(L2)] for Neu5Ac (Keq = 151) over D-(+)-glucose (Keq = 12.3), D-mannose (Keq = 21.9), and D-galactose (Keq = 24.5). Also, a very weak binding affinity was observed in the case of Me α-D-galactoside and Me α-D-mannoside. An 8-fold increase of the binding constant of [Gd(L2)] with Neu5Ac is observed when compared to that of PBA determined under the same conditions (Keq = 19). 13C NMR spectroscopy and d. functional theory calculations performed at the B3LYP/6-31G(d) level show that this is due to a cooperative two-site binding of Neu5Ac through (1) ester formation by interaction on the PBA function of the receptor and (2) coordination of the carboxylate group of Neu5Ac to the GdIII ion. The emission lifetime of the 5D4 level of TbIII in [Tb(L2)] increases upon Neu5Ac binding, in line with the displacement of inner-sphere water mols. due to coordination of Neu5Ac to the metal ion.

Inorganic Chemistry published new progress about 166821-88-1. 166821-88-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Boronic acid and ester,Benzyl bromide,Benzene,Boronic Acids,Boronic acid and ester, name is 2-(2-(Bromomethyl)phenyl)-5,5-dimethyl-1,3,2-dioxaborinane, and the molecular formula is C12H16BBrO2, SDS of cas: 166821-88-1.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Cheng, Haojin’s team published research in Canadian Journal of Chemistry in 88 | CAS: 52431-30-8

Canadian Journal of Chemistry published new progress about 52431-30-8. 52431-30-8 belongs to bromides-buliding-blocks, auxiliary class Liquid Crystal &OLED Materials, name is 2,5-Dibromo-3,4-dinitrothiophene, and the molecular formula is C4Br2N2O4S, Quality Control of 52431-30-8.

Cheng, Haojin published the artcileIron(II) complexes containing thiophene-substituted “bispicen” ligands – Spin-crossover, ligand rearrangements, and ferromagnetic interactions, Quality Control of 52431-30-8, the publication is Canadian Journal of Chemistry (2010), 88(9), 954-963, database is CAplus.

The synthesis and characterization of three new tetradentate bispicen-type ligands containing a substituted thiophene heterocycle [I, R = H (7), Ph (8), or 2-thienyl (9)] are described. Iron(II) bis(thiocyanate) coordination complexes containing 79 were prepared, and the electronic and variable-temperature magnetic properties of complexes containing 7 (10) and 9 (12) are described. Complex 10 features a gradual and incomplete spin crossover in the solid state, and 12 remains high-spin over the entire temperature range. Complex 11 containing 8 is extremely unstable and rearranges to another iron(II) complex (13), which was structurally characterized. The temperature-dependent magnetic properties of 13 are described as a 1-dimensional ferromagnetic chain, with interchain antiferromagnetic interactions and (or) zero-field splitting dominant at low temperatures The magnetic anal. is corroborated by the mol. packing and d. functional theory calculations, which suggest intermol. interactions between coordinated thiocyanate ligands bearing a significant spin d.

Canadian Journal of Chemistry published new progress about 52431-30-8. 52431-30-8 belongs to bromides-buliding-blocks, auxiliary class Liquid Crystal &OLED Materials, name is 2,5-Dibromo-3,4-dinitrothiophene, and the molecular formula is C4Br2N2O4S, Quality Control of 52431-30-8.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Orthgiess, Erhard’s team published research in Tenside, Surfactants, Detergents in 27 | CAS: 518-67-2

Tenside, Surfactants, Detergents published new progress about 518-67-2. 518-67-2 belongs to bromides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Benzene, name is Dimidium bromide, and the molecular formula is C20H18BrN3, Application of Dimidium bromide.

Orthgiess, Erhard published the artcileColorimetric determination of anionic surfactants, Application of Dimidium bromide, the publication is Tenside, Surfactants, Detergents (1990), 27(4), 226-8, database is CAplus.

A method for the determination of anionic surfactants such as alkyl- and alkylarylsulfates, -sulfonates, and -sulfosuccinates in aqueous solutions is based on the absorbance measurement of surfactant-dye (i.e., 3,8-diamino-5-methyl-6-phenylphenanthridinium bromide) complexes at 525 nm. The technique is simpler and faster than other colorimetric methods and can be used for the anal. of 1 × 10-4 to 5 × 10-7 M solutions

Tenside, Surfactants, Detergents published new progress about 518-67-2. 518-67-2 belongs to bromides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Benzene, name is Dimidium bromide, and the molecular formula is C20H18BrN3, Application of Dimidium bromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Shimada, Kazutake et al. published their research in Journal of Chromatography, Biomedical Applications in 1991 | CAS: 80480-15-5

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) belongs to organobromine compounds. Many of the organo bromine compounds are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5) and hence the carbon in a carbon–bromine bond is electrophilic in nature. The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.COA of Formula: C18H11BrO

High-performance liquid chromatographic separation of bile acid pyrenacyl esters with cyclodextrin-containing mobile phase was written by Shimada, Kazutake;Komine, Yoshihiro;Mitamura, Kuniko. And the article was included in Journal of Chromatography, Biomedical Applications in 1991.COA of Formula: C18H11BrO The following contents are mentioned in the article:

Compared with conventional methods, inclusion chromatog. gives much more satisfactory separation of 1-bromoacetylpyrene-derivatized bile acids in a short time. The application of this method to the separation of glycine-conjugated bile acids in human bile is described. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5COA of Formula: C18H11BrO).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) belongs to organobromine compounds. Many of the organo bromine compounds are relatively nonpolar. Bromine is more electronegative than carbon (2.8 vs 2.5) and hence the carbon in a carbon–bromine bond is electrophilic in nature. The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.COA of Formula: C18H11BrO

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Sakurai, Tadamitsu et al. published their research in Journal of the Chemical Society, Chemical Communications in 1995 | CAS: 80480-15-5

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.SDS of cas: 80480-15-5

The role of papain in the association process of a 1-pyrenoyl pendant attached to its active site was written by Sakurai, Tadamitsu;Watanabe, Kenichiro;Nojima, Kazue;Inoue, Hiroyasu. And the article was included in Journal of the Chemical Society, Chemical Communications in 1995.SDS of cas: 80480-15-5 The following contents are mentioned in the article:

An anal. of the spectroscopic behavior of papain modified by 1-bromoacetylpyrene demonstrates that the active site of this enzyme remarkably promotes the formation of the ground-state dimer derived from the pyrenoyl pendant covalently bound to the cysteine-25 residue. This study involved multiple reactions and reactants, such as 2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5SDS of cas: 80480-15-5).

2-Bromo-1-(pyren-1-yl)ethanone (cas: 80480-15-5) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.SDS of cas: 80480-15-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhang, Chun-Lin et al. published their research in Organic Letters in 2016 | CAS: 1890136-54-5

2-Bromo-5′-phenyl-1,1′:3′,1”-terphenyl (cas: 1890136-54-5) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.COA of Formula: C24H17Br

N-Heterocyclic Carbene-Catalyzed Construction of 1,3,5-Trisubstituted Benzenes from Bromoenals and α-Cyano-β-methylenones was written by Zhang, Chun-Lin;Ye, Song. And the article was included in Organic Letters in 2016.COA of Formula: C24H17Br The following contents are mentioned in the article:

A direct and efficient approach to 1,3,5-trisubstituted benzenes has been developed via N-heterocyclic carbene-catalyzed [2 + 4] annulation of α-bromoenals and α-cyano-β-methylenones. The reaction worked well for both aryl- and alkylenones. This study involved multiple reactions and reactants, such as 2-Bromo-5′-phenyl-1,1′:3′,1”-terphenyl (cas: 1890136-54-5COA of Formula: C24H17Br).

2-Bromo-5′-phenyl-1,1′:3′,1”-terphenyl (cas: 1890136-54-5) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.COA of Formula: C24H17Br

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wang, Lei et al. published their research in Synthesis in 2018 | CAS: 922721-30-0

3-Bromo-9-(4-fluorophenyl)-9H-carbazole (cas: 922721-30-0) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Application In Synthesis of 3-Bromo-9-(4-fluorophenyl)-9H-carbazole

Corrigendum to Site-Selective N-Arylation of Carbazoles with Halogenated Fluorobenzenes [Erratum to document cited in CA164:251427] was written by Wang, Lei;Ji, Enhui;Liu, Ning;Dai, Bin. And the article was included in Synthesis in 2018.Application In Synthesis of 3-Bromo-9-(4-fluorophenyl)-9H-carbazole The following contents are mentioned in the article:

A reference was left out, as well as an in-text citation for it. The corrections are provided. This study involved multiple reactions and reactants, such as 3-Bromo-9-(4-fluorophenyl)-9H-carbazole (cas: 922721-30-0Application In Synthesis of 3-Bromo-9-(4-fluorophenyl)-9H-carbazole).

3-Bromo-9-(4-fluorophenyl)-9H-carbazole (cas: 922721-30-0) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Application In Synthesis of 3-Bromo-9-(4-fluorophenyl)-9H-carbazole

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wong, Wi-Yeung et al. published their research in Angewandte Chemie, International Edition in 2007 | CAS: 922721-30-0

3-Bromo-9-(4-fluorophenyl)-9H-carbazole (cas: 922721-30-0) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Category: bromides-buliding-blocks

Multifunctional iridium complexes based on carbazole modules as highly efficient electrophosphors. [Erratum to document cited in CA146:389911] was written by Wong, Wi-Yeung;Ho, Cheuk-Lam;Gao, Zhi-Qiang;Mi, Bao-Xiu;Chen, Chin-Hsin;Cheah, Kok-Wai;Lin, Zhenyang. And the article was included in Angewandte Chemie, International Edition in 2007.Category: bromides-buliding-blocks The following contents are mentioned in the article:

The chem. structures of 1 and 2 in Scheme 1 were incorrect. The correct structures are given. This study involved multiple reactions and reactants, such as 3-Bromo-9-(4-fluorophenyl)-9H-carbazole (cas: 922721-30-0Category: bromides-buliding-blocks).

3-Bromo-9-(4-fluorophenyl)-9H-carbazole (cas: 922721-30-0) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. Commercially available organobromine pharmaceuticals include the vasodilator nicergoline, the sedative brotizolam, the anticancer agent pipobroman, and the antiseptic merbromin. Category: bromides-buliding-blocks

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary