39145-33-0

Basic information

• Product Name: 2-Propenethioamide, 3-(4-chlorophenyl)-2-cyano-
• CAS NO: 39145-33-0
• Molecular Formula: C10H7ClN2S
• Molecular Weight: 222.698
• Mol File: 39145-33-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propenethioamide, 3-(4-chlorophenyl)-2-cyano-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenethioamide, 3-(4-chlorophenyl)-2-cyano-(39145-33-0)
• EPA Substance Registry System: 2-Propenethioamide, 3-(4-chlorophenyl)-2-cyano-(39145-33-0)

Safety Data

• Hazardous Substances Data: 39145-33-0(Hazardous Substances Data)

Upstream product

• 7357-70-2 Cyanothioacetamide 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 148859-86-3 4-(4-Chloro-phenyl)-5-cyano-6-mercapto-2-methyl-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester; compound with piperidine 
• 97651-28-0 ethyl 4-(4'-chlorophenyl)-3-cyano-6-methyl-1,2-dihydropyridine-5-carboxylate 
• 97651-08-6 4-(4-Chloro-phenyl)-5-cyano-2-methyl-6-thioxo-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester 
• 100219-51-0 cis-3-Cyano-4-(p-chlorophenyl)-5-methoxycarbonyl-6-methyl-3,4-dihydropyridine-2-thione 
• 100219-51-0 trans-3-Cyano-4-(p-chlorophenyl)-5-methoxycarbonyl-6-methyl-3,4-dihydropyridine-2-thione 
• 6265-91-4 2-(4-chlorophenyl)benzothiazole 
• 164025-19-8 (Z)-3-(4-Chloro-phenyl)-2-(4-methyl-5-phenylazo-thiazol-2-yl)-acrylonitrile 
• 200339-95-3 4-(4-Chloro-phenyl)-7,7-dimethyl-5-oxo-2-thioxo-1,2,5,6,7,8-hexahydro-quinoline-3-carbonitrile 
• 213883-28-4 4-(4-Chloro-phenyl)-5-cyano-2-oxo-6-thioxo-1,2,3,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester 
• 1867-38-5 4-chlorobenzylidenemalonodinitrile 
• 103868-29-7 5-acetyl-6-methyl-4-(4-chlorophenyl)-3-cyano-2<1H>pyridinethione 
• 103868-26-4 5-acetyl-6-methyl-4-(4-chlorophenyl)-3-cyano-3,4-dihydro-2<1H>pyridinethione 
• 82127-15-9 4-(4-chlorophenyl)-6-(thien-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile 
• 210287-81-3 C₂₅H₁₃ClN₂O₂S 

Relevant articles and documents

Novel multicomponent synthesis of 6,7-dihydro-5H-cyclopenta[b]pyridine derivatives

[Figure not available: see fulltext.] The multicomponent condensation of malononitrile, hydrogen sulfide, aldehydes, 1-(cyclopent-1-en-1-yl)pyrrolidine, and alkylating agents leads to the formation of 6,7-dihydro-5H-cyclopenta[b]pyridine derivatives. The structure of a number of heterocycles obtained on their basis was studied by X-ray structural analysis.

New Multicomponent Synthesis of Functionalized Nitriles and Esters of 6-Alkylsulfanyl-1,4-dihydronicotinic Acids

Abstract: The multicomponent condensation of malononitrile, hydrogen sulfide, aryl orhetaryl aldehydes, 1,3-dicarbonyl compounds and alkylating reagents affordedfunctionalized nitriles and esters of 6-alkylsulfanyl-1,4-dihydronicotinicacids, their aromatic analogues and 1,4-dihydrothieno[2,3-b]pyridines.

Condensation of α-cyanothioacetamide with aldehydes catalyzed by Envirocat EPZG

Condensation of α-cyanothioacetamide with aldehydes has been carried out in excellent yield under mild conditions by using Envirocat EPZG as a heterogenous reusable catalyst.