39145-31-8

Basic information

• Product Name: 2-Propenethioamide, 2-cyano-3-(4-methoxyphenyl)-
• CAS NO: 39145-31-8
• Molecular Formula: C11H10N2OS
• Molecular Weight: 218.279
• Mol File: 39145-31-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-Propenethioamide, 2-cyano-3-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenethioamide, 2-cyano-3-(4-methoxyphenyl)-(39145-31-8)
• EPA Substance Registry System: 2-Propenethioamide, 2-cyano-3-(4-methoxyphenyl)-(39145-31-8)

Safety Data

• Hazardous Substances Data: 39145-31-8(Hazardous Substances Data)

Upstream product

• 7357-70-2 Cyanothioacetamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 2826-26-8 2-(4-methoxyphenylmethylene)malononitrile 
• 19172-47-5 Lawessons reagent 

Downstream Products

• 85460-35-1 1-Amino-3-(4-methoxyphenyl)-3H-pyrido<2,1-b>benzothiazol-2,4-dicarbonitrile 
• 115071-99-3 α-(4-phenylcarbamoylmethyl-2-thiazolyl)-p-chlorocinnamonitrile 
• 128342-34-7 6-(4-Methoxy-phenyl)-2-thioxo-4-p-tolyl-1,2-dihydro-pyridine-3-carbonitrile 
• 108463-39-4 C₃₉H₃₆N₆O₅S₂ 
• 97651-29-1 ethyl 3-cyano-1,2-dihydro-4-p-methoxyphenyl-6-methyl-2-thioxopyridin-4-carboxylate 
• 97651-29-1 5-Cyano-6-mercapto-4-(4-methoxy-phenyl)-2-methyl-nicotinic acid ethyl ester 
• 108463-32-7 5-Cyano-6-mercapto-4-(4-methoxy-phenyl)-2-methyl-3,4-dihydro-pyridine-3-carboxylic acid phenylamide 
• 102423-77-8 1,2-dihydro-6-hydroxy-4-(4-methoxyphenyl)-2-thioxo-3,5-pyridinedicarbonitrile 
• 129226-96-6 6-(2-Amino-phenylsulfanyl)-4-(4-methoxy-phenyl)-2-thioxo-1,2-dihydro-pyridine-3,5-dicarbonitrile 
• 204988-86-3 4-(4-Methoxy-phenyl)-5-[(E)-phenylimino]-2-thioxo-2,5-dihydro-1H-indeno[1,2-b]pyridine-3-carbonitrile 
• 121104-38-9 5-acetyl-3-cyano-4-(4-methoxyphenyl)-6-methylpyridine-2(1H)-thione 
• 189952-03-2 5-acetyl-4-(4-methoxy-phenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydro-pyridine-3-carbonitrile 
• 264195-72-4 2-hydrazino-7-(4-methoxy-phenyl)-5-oxo-5H-pyrano[2,3-d]thiazole-6-carbothioic acid amide 
• 264195-74-6 2-hydrazino-7-(4-methoxy-phenyl)-6-(4-oxo-4,5-dihydro-thiazol-2-yl)-pyrano[2,3-d]thiazol-5-one 

Relevant articles and documents

Multicomponent Synthesis and Molecular and Crystal Structure of New Derivatives of Partially Hydrogenated Quinolines

Abstract: The multicomponent condensation of aromatic aldehydes, cyanothioacetamide, 1-(cyclohex-1-en-1-yl)azepine, and α-halocarbonyl compounds was studied. As a result, new derivatives of partially hydrogenated quinolines were synthesized. The molecular and crystal structures of a number of the synthesized heterocycles were studied X-ray analysis.

Design and synthesis of pyrido[2,1- b ][1,3,5]thiadiazine library via uncatalyzed mannich-type reaction

This Research Article describes the synthesis of an over 700-member library of (8R/8S)-3-R-8-aryl-6-oxo-3,4,7,8-tetrahydro-2H,6H-pyrido[2,1-b][1,3,5]thiadiazin-9-carbonitriles by uncatalyzed Mannich-type reaction of N-methylmorpholinium (4R/4S)-4-aryl-3-cyano-6-oxo-1,4,5,6-tetrahydropyridin-2-thiolates with a set of primary amines and excessive HCHO. The scope and limitations of the reaction were studied. Starting thiolates were obtained in yields of 53-82% by multicomponent reaction of aromatic aldehydes, cyanothioacetamide, 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid), and N-methylmorpholine, followed by heterocyclization of the resulting Michael adducts.

The behaviour of arylidenemalononitriles towards certain thiating phosphorus reagents

The behaviour of arylidenemalononitriles 1, 2 and 3 towards certain thiating phosphorus reagents, namely, phosphorus pentasulfide and Lawesson's reagent 10, has been outlined. The products obtained depend on the nature of reactants. Analytical and spectro