CAS 18982-54-2
:Álcool 2-bromobenzílico
- (2-Bromophenyl)Methanol
- 1-Bromo-2-(hydroxymethyl)benzene
- 2-(Hydroxymethyl)phenyl bromide
- 2-Bromobenzenemethanol
- 2-Bromophenylmethanol
- 2-Hydroxymethyl-1-bromobenzene
- Benzenemethanol, 2-bromo-
- Benzyl alcohol, o-bromo-
- O-Bromobenzyl Alcohol
- 2-Bromobenzyl alcohol
2-Bromobenzyl Alcohol
CAS:Fórmula:C7H7BrOPureza:>99.0%(GC)Cor e Forma:White to Almost white powder to crystalPeso molecular:187.042-Bromobenzyl alcohol, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Fórmula:C7H7BrOPureza:98%Cor e Forma:White to cream, Crystals or powder or crystalline powder or fused solidPeso molecular:187.042-Bromobenzyl alcohol
CAS:2-Bromobenzyl alcohol
Fórmula:C7H7BrOPureza:98%Cor e Forma: white to off-white solidPeso molecular:187.03g/mol2-Bromobenzyl alcohol
CAS:2-Bromobenzyl alcohol is an organic compound that contains a benzyl group, a hydroxyl group, and a bromine atom. It has been shown to be an effective catalyst for the cross-coupling of organic halides with alkyl Grignard reagents in the presence of sodium carbonate. The reaction mechanism involves formation of an intermolecular hydrogen bond between the carbonyl group and the 2-bromobenzyl alcohol. This reaction produces a constant that can be used to calculate the population growth rate. 2-Bromobenzyl Alcohol has optical properties that are similar to those of water, which makes it suitable for applications such as fuel cells or sensors.Fórmula:C7H7BrOPureza:Min. 95%Cor e Forma:PowderPeso molecular:187.03 g/mol2-Bromobenzyl Alcohol
CAS:Produto ControladoApplications 2-Bromobenzyl Alcohol acts as a reagent for the synthesis of alkoxy tetrasubstituted chiral amino acids via three-component reaction of (diazo)oxindoles, alcohols and benzhydrylimino ester involving enantioselective trapping of oxonium ylides by benzhydrylimino ester. Also acts as a reagent for the preparation of orally active and liver-targeted prodrug of 5-fluoro-2'-deoxyuridine for treatment of hepatocellular carcinoma.
References Jia, S., et al.: Chin. Chem. Lett., PagesAhead of Print (2016); Peng, Y., et al.: J. Med. Chem., 59, 3661 (2016)Fórmula:C7H7BrOCor e Forma:NeatPeso molecular:187.03







