7141-05-1

Basic information

• Product Name: Benzenemethanol, 2-amino-5-bromo-a-phenyl-
• Synonyms: 2-Amino-5-brom-benzhydrol;2-amino-5-bromo-benzhydrol;5-Brom-2-amino-benzhydrol
• CAS NO: 7141-05-1
• Molecular Formula: C13H12BrNO
• Molecular Weight: 278.148
• Mol File: 7141-05-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-amino-5-bromo-a-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-amino-5-bromo-a-phenyl-(7141-05-1)
• EPA Substance Registry System: Benzenemethanol, 2-amino-5-bromo-a-phenyl-(7141-05-1)

Safety Data

• Hazardous Substances Data: 7141-05-1(Hazardous Substances Data)

Upstream product

• 591-51-5 phenyllithium 
• 5794-88-7 5-Bromo-2-aminobenzoic acid 
• 39859-36-4 2-amino-5-bromobenzophenone 
• 29124-57-0 2-amino-5-bromobenzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 552-89-6 2-nitro-benzaldehyde 
• 88092-64-2 2-Acetylamino-3,5-dibromobenzophenone 
• 2243-79-0 2-nitrobenzophenone 
• 64-17-5 ethanol 
• 69751-74-2 (2-amino-3,5-dibromophenyl)phenylmethanone 

Downstream Products

• 101868-25-1 (2-amino-5-bromophenyl)diphenylmethanol 
• 1229609-99-7 6-bromo-2,4-diphenylquinazoline 
• 305864-80-6 6-bromo-4-phenylquinazoline 
• 39859-36-4 2-amino-5-bromobenzophenone 
• 104542-54-3 2-(N-carbobenzoxyglycyl-glycyl)amido-5-bromobenzhydrol 
• 13209-38-6 (2-aminophenyl)(phenyl)methanol 

Relevant articles and documents

DIHYDROQUINAZOLINONE ANALOGUES AS BRD4 INHIBITORS

The present invention encompasses compounds of general formula (I) wherein the groups R1 to R4 and A1 to A5 have the meanings given in the claims and in the specification. The compounds of the invention are suitable for the treatment of diseases characterized by excessive or abnormal cell proliferation pharmaceutical preparations containing such compounds and their uses as a medicament.

Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity

A novel metal-free intramolecular oxidative decarboxylative coupling of primary α-amino acids with 2-aminobenzoketones under mild and neutral conditions was developed. Different quinazolines can be selectively obtained by various oxidants.