254114-95-9

Basic information

• Product Name: (para-bromophenyl)diethylphosphonoacetate
• Synonyms: (para-bromophenyl)diethylphosphonoacetate
• CAS NO: 254114-95-9
• Molecular Weight: 351.134
• Mol File: 254114-95-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (para-bromophenyl)diethylphosphonoacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (para-bromophenyl)diethylphosphonoacetate(254114-95-9)
• EPA Substance Registry System: (para-bromophenyl)diethylphosphonoacetate(254114-95-9)

Safety Data

• Hazardous Substances Data: 254114-95-9(Hazardous Substances Data)

Upstream product

• 3095-95-2 diethylphosphonoacetic acid 
• 106-41-2 4-bromo-phenol 

Downstream Products

• 254115-09-8 (para-bromophenyl)-6-chloro-2-(E)-hexenoate 
• 227946-96-5 (para-bromophenyl)-4-methyl-2-(E)-pentenoate 
• 254115-08-7 (para-bromophenyl)-2-(E)-butenoate 
• 50663-21-3 (para-bromophenyl)-2-propenoate 
• 254115-13-4 (2S,3R)-(para-bromophenyl)-2-benzylcarbamate-3-hydroxy-6-chlorohexenoate 
• 298199-44-7 (2S,3R)-(para-bromophenyl)-2-benzylcarbamate-3-hydroxy-6-chlorohexanoate 
• 298199-45-8 (2S,3R)-6-Azido-2-benzyloxycarbonylamino-3-hydroxy-hexanoic acid 4-bromo-phenyl ester 

Relevant articles and documents

An asymmetric aminohydroxylation approach to the azepine core of (-)-balanol

(equation presented) An efficient formal synthesis of the potent protein kinase C inhibitor (-)-balanol that relies on a modified asymmetric aminohydroxylation of the α,β-unsaturated aryl ester (1) is reported. The aryl ester functionality and the dihydroquinyl alkaloid ligand system (DHQ)2-AQN are used to control the regio- and enantioselectivity of the process.