115706-16-6

Basic information

• Product Name: methyl 2-bromo-3-(3,4-dichlorophenyl)propionate
• Synonyms: methyl 2-bromo-3-(3,4-dichlorophenyl)propionate
• CAS NO: 115706-16-6
• Molecular Weight: 311.99
• Mol File: 115706-16-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl 2-bromo-3-(3,4-dichlorophenyl)propionate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-bromo-3-(3,4-dichlorophenyl)propionate(115706-16-6)
• EPA Substance Registry System: methyl 2-bromo-3-(3,4-dichlorophenyl)propionate(115706-16-6)

Safety Data

• Hazardous Substances Data: 115706-16-6(Hazardous Substances Data)

Upstream product

• 95-76-1 m,p-dichloroaniline 
• 292638-85-8 acrylic acid methyl ester 

Downstream Products

• 75416-52-3 6,7-dichloro-1,2,3,4-tetrahydroisoquinoline 
• 115706-18-8 1,2-dichloro-4-(2-isocyanatoethyl)benzene 
• 115706-19-9 6,7-dichloro-1,2,3,4-tetrahydro-1-oxoisoquinoline 
• 90273-67-9 3-(3,4-dichlorophenyl)propionic acid chloride 
• 25173-68-6 3(3,4-dichlorophenyl)propanoic acid 
• 115706-17-7 methyl 3‐(3,4‐dichlorophenyl)propanoate 

Relevant articles and documents

Synthesis of Oxazine, Thiazine, and Quinoxaline Derivatives Containing a Benzyl Fragment from 3-Aryl-2-Bromopropanoic Acids and Their Esters

Abstract: 3-Aryl-2-bromopropanoic acid esters reacted with o-phenylenediamine, 2-sulfanylaniline, and L-cysteine to give quinoxaline, 1,4-thiazine, and thiomorpholine derivatives, respectively, containing an aryl-methyl substituent. Analogous 1,4-benzoxaz

One-pot synthesis of alkyl 3-aryl-2-(4-phenyl-1H-1,2,3-triazol-1-yl)propanoates

Reaction of 3-aryl-2-bromopropanoic acids esters, products of the Meerwein arylation, with sodium azide afforded alkyl 2-azido-3-arylpropanoates. The latter react with ethyl acetoacetate and phenylacetylene to form 1,2,3-triazole derivatives. A one-pot me