99955-80-3

Basic information

• Product Name: N-<2-(4-Methoxyphenyl)-1-thioxoethyl>piperidine
• Synonyms: N-<2-(4-Methoxyphenyl)-1-thioxoethyl>piperidine
• CAS NO: 99955-80-3
• Molecular Weight: 249.377
• Mol File: 99955-80-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-<2-(4-Methoxyphenyl)-1-thioxoethyl>piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-<2-(4-Methoxyphenyl)-1-thioxoethyl>piperidine(99955-80-3)
• EPA Substance Registry System: N-<2-(4-Methoxyphenyl)-1-thioxoethyl>piperidine(99955-80-3)

Safety Data

• Hazardous Substances Data: 99955-80-3(Hazardous Substances Data)

Upstream product

• 81860-76-6 2-(4-methoxyphenyl)-1-(piperidin-1-yl)ethan-1-one 
• 110-89-4 piperidine 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 114393-72-5 (Z)-Methyl <2-(4-Methoxyphenyl)-1-(methylthio)ethylidene>hydrazinocarboxylate 
• 114393-73-6 (E)-Methyl <2-(4-Methoxyphenyl)-1-(methylthio)ethylidene>hydrazinocarboxylate 
• 114393-29-2 3-[[5-(4-methoxyphenyl)-1,2,3-thiadiazol-4-yl]thio]propanoic acid, ethyl ester 
• 114373-71-6 N'-[2-(4-Methoxy-phenyl)-thioacetyl]-hydrazinecarboxylic acid methyl ester 
• 114373-72-7 Ethyl <<2-(4-Methoxyphenyl)-1-thioxoethyl>thio>acetate 
• 114393-71-4 5-(4-Methoxyphenyl)-4-(methylthio)-1,2,3-thiadiazole 
• 76579-50-5 methyl 4'-methoxy-2-phenylethanedithioate 
• 81860-76-6 2-(4-methoxyphenyl)-1-(piperidin-1-yl)ethan-1-one 
• 82966-18-5 1-(4-methoxyphenethyl)-piperidine 

Relevant articles and documents

Decarboxylative thioamidation of arylacetic and cinnamic acids: A new approach to thioamides

A new decarboxylative strategy has been developed for the synthesis of thioamides via a three-component reaction involving arylacetic or cinnamic acids, amines and elemental sulfur powder, without the need of a transition metal and an external oxidant.

Reactions of N,N-(dialkyl)arylthioacetamides with dialkyl acetylenedicarboxylates

2-(Alkoxycarbonylmethylidene)-4-aryl-5-(dialkylamino)thiophen-3(2H)-ones were synthesized by condensation of N,N-(dialkyl)arylthioacetamides with dialkyl acetylenedicarboxylates. Intermediate substituted vinylic sulfides were isolated. When heated or in t