443361-07-7

Basic information

• Product Name: (2-(benzylamino)-5-bromophenyl)methanol
• Synonyms: (2-(benzylamino)-5-bromophenyl)methanol
• CAS NO: 443361-07-7
• Molecular Weight: 292.175
• Mol File: 443361-07-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (2-(benzylamino)-5-bromophenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-(benzylamino)-5-bromophenyl)methanol(443361-07-7)
• EPA Substance Registry System: (2-(benzylamino)-5-bromophenyl)methanol(443361-07-7)

Safety Data

• Hazardous Substances Data: 443361-07-7(Hazardous Substances Data)

Upstream product

• 1131587-77-3 methyl 2-(benzylamino)-5-bromobenzoate 
• 100-44-7 benzyl chloride 
• 52727-57-8 5-bromo-2-aminobenzoic acid methyl ester 
• 98-88-4 benzoyl chloride 
• 307539-90-8 methyl 2-benzamido-5-bromobenzoate 

Downstream Products

• 1201939-24-3 2-(benzylamino)-5-bromobenzaldehyde 
• 443361-08-8 N-benzyl-N-(4-bromo-2-formylphenyl)acrylamide 
• 911136-85-1 N-benzyl-N-(4-bromo-2-hydroxymethylphenyl)acrylamide 

Relevant articles and documents

Synthesis of substituted indole from 2-aminobenzaldehyde through [1,2]-aryl shift

A mild, efficient, and simple method for the synthesis of 3-ethoxycarbonylindoles has been developed. Addition of ethyl diazoacetate (EDA) to 2-aminobenzaldehydes cleanly affords the indole core. As opposed to other common approaches for the synthesis of indole, this method displays both excellent functional group tolerance and perfect regiochemical control. This allowed the synthesis of a variety of useful indole building blocks from 2-aminobenzaldehydes derived from readily available anthranilic acids.

Cyclization reactions of N-acryloyl-2-aminobenzaldehyde derivatives: formal total synthesis of martinellic acid

N-Alkyl acryloylamides derived from o-aminobenzaldehyde derivatives react with N-alkyl glycine derivatives to provide cis-fused pyrrole[3,2-c]quinolones in moderate yield and high diastereoselectivity. These same substrates engage in a tandem Michael-Mann