81860-94-8

Basic information

• Product Name: 3-(Bromomethyl)-4-methoxyphenyl acetate
• Synonyms: 3-(Bromomethyl)-4-methoxyphenyl acetate
• CAS NO: 81860-94-8
• Molecular Weight: 0
• Mol File: 81860-94-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(Bromomethyl)-4-methoxyphenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Bromomethyl)-4-methoxyphenyl acetate(81860-94-8)
• EPA Substance Registry System: 3-(Bromomethyl)-4-methoxyphenyl acetate(81860-94-8)

Safety Data

• Hazardous Substances Data: 81860-94-8(Hazardous Substances Data)

Upstream product

• 84923-68-2 5-(benzyloxy)-2-methoxybenzoic acid 
• 61227-25-6 2-methoxy-5-hydroxybenzoic acid 
• 87513-63-1 5-Hydroxy-2-methoxybenzoesaeure-methylester 
• 52329-04-1 5-Benzyloxy-2-methoxybenzoesaeure-methylester 
• 506-96-7 Acetyl bromide 
• 87633-45-2 5-Hydroxy-2-methoxybenzylalkohol 

Downstream Products

• 81860-99-3 N-tert-Butoxycarbonyl-cis-3-(3-cyanmethyl-4-methoxyphenoxy)prolin-methylester 
• 81860-99-3 N-tert-Butoxycarbonyl-trans-3-(3-cyanmethyl-4-methoxyphenoxy)prolin-methylester 
• 87633-47-4 N-tert-Butoxycarbonyl-trans-3-(3-cyanmethyl-4-methoxyphenoxy)prolin 
• 87633-47-4 cis/trans-N-tert-Butoxycarbonyl-3-(3-cyanmethyl-4-methoxyphenoxy)prolin 
• 81860-92-6 (2S,3S)-3-(3-{2-[((S)-1-Benzyloxycarbonyl-pyrrolidine-2-carbonyl)-amino]-ethyl}-4-methoxy-phenoxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-pentafluorophenyl ester 
• 81860-91-5 (2R,3R)-3-(3-{2-[((R)-1-Benzyloxycarbonyl-pyrrolidine-2-carbonyl)-amino]-ethyl}-4-methoxy-phenoxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 
• 81860-97-1 3-(3-Cyanmethyl-4-methoxyphenoxy)prolin 
• 81860-95-9 5-Hydroxy-2-methoxybenzylcyanid 
• 81860-97-1 cis-3-(3-Cyanmethyl-4-methoxyphenoxy)prolin 
• 81860-97-1 trans-3-(3-Cyanmethyl-4-methoxyphenoxy)prolin 
• 81860-96-0 3-(3-Cyanmethyl-4-methoxyphenoxy)-1-pyrrolin-2-carbonsaeure-methylester 

Relevant articles and documents

Syntheses of Peptide Alkaloids, VII. - Amino Acids and Peptides, XXXVIII. - Total Synthesis of the 10,11-Dihydrozizyphines A and B

The 10,11-dihydrozizyphines A (13a) and B (15a) were synthesized.The cyclopeptide ring closure reactions were accomplished by catalytic hydrogenation of the linear ω-Z-amino acid pentafluorophenyl ester 8a.