55164-19-7

Basic information

• Product Name: 2-Propenoic acid, 3-chloro-3-phenyl-, ethyl ester, (Z)-
• CAS NO: 55164-19-7
• Molecular Formula: C11H11ClO2
• Molecular Weight: 210.66
• Mol File: 55164-19-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-chloro-3-phenyl-, ethyl ester, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-chloro-3-phenyl-, ethyl ester, (Z)-(55164-19-7)
• EPA Substance Registry System: 2-Propenoic acid, 3-chloro-3-phenyl-, ethyl ester, (Z)-(55164-19-7)

Safety Data

• Hazardous Substances Data: 55164-19-7(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 85311-59-7 (E)-3-Chloro-3-phenyl-acryloyl chloride 
• 18819-66-4 (Z)-3-chloro-3-phenyl-2-propenoic acid 
• 623-73-4 diazoacetic acid ethyl ester 
• 4460-46-2 3-chloro-3-phenyl-3H-diazirine 
• 637-44-5 phenylpropyolic acid 
• 2216-94-6 phenylpropynoic acid ethyl ester 

Downstream Products

• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 128671-30-7 (Z)-3-(2,5-Dimethoxy-phenylsulfanyl)-3-phenyl-acrylic acid ethyl ester 
• 128671-29-4 (E)-3-(2,5-Dimethoxy-phenylsulfanyl)-3-phenyl-acrylic acid ethyl ester 
• 84144-37-6 ethyl (Z)-3-((4-methoxyphenyl)thio)cinnamate 
• 128671-25-0 ethyl (Z)-3-((4-chlorophenyl)thio)-3-phenylacrylate 
• 128671-31-8 (E)-3-(4-Chloro-phenylsulfanyl)-3-phenyl-acrylic acid ethyl ester 
• 128671-22-7 3,3-Bis-(4-methoxy-phenylsulfanyl)-3-phenyl-propionic acid ethyl ester 
• 128671-24-9 3,3-Bis-(4-chloro-phenylsulfanyl)-3-phenyl-propionic acid ethyl ester 
• 128671-21-6 3-Phenyl-3,3-bis-p-tolylsulfanyl-propionic acid ethyl ester 
• 128671-23-8 β-(4-methoxy-phenylsulfanyl)-cinnamic acid ethyl ester 
• 34875-04-2 β-p-tolylsulfanyl-trans-cinnamic acid ethyl ester 
• 34875-14-4 cis-β-p-Tolylthio-zimtsaeureethylester 
• 34875-02-0 ethyl (Z)-3-phenyl-3-(phenylthio)acrylate 
• 34875-12-2 ethyl (E)-3-phenyl-3-(phenylthio)acrylate 

Relevant articles and documents

Chloride-tolerant gold(I)-catalyzed regioselective hydrochlorination of alkynes

We have developed a highly regioselective homogeneous gold(I)-catalyzed anti-hydrochlorination of unactivated alkynes at room temperature. We have overcome the incompatibility between conventional cationic gold catalysts and chloride by using a hydrogen-b

Stereochemistry of the Reactions of CuI Catalyzed Grignard Reagents with Ethyl (E)- and (Z)-β-Chlorocinnamates

Ethyl (E)- and (Z)-3-chloro-3-phenyl-2-propenoate were prepared and separated.The (Z)-isomer gave β-alkylated ethyl cinnamates in good yield when reacted with alkyl Grignard reagents in the presence of 10percent CuI.The (Z)-isomer reacted with retention o