115969-26-1

Basic information

• Product Name: [2-Azepan-1-yl-4-(4-nitro-phenyl)-thiazol-5-yl]-(4-methoxy-phenyl)-methanone
• Synonyms: [2-Azepan-1-yl-4-(4-nitro-phenyl)-thiazol-5-yl]-(4-methoxy-phenyl)-methanone
• CAS NO: 115969-26-1
• Molecular Weight: 437.519
• Mol File: 115969-26-1.mol

Chemical Properties

• CAS DataBase Reference: [2-Azepan-1-yl-4-(4-nitro-phenyl)-thiazol-5-yl]-(4-methoxy-phenyl)-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: [2-Azepan-1-yl-4-(4-nitro-phenyl)-thiazol-5-yl]-(4-methoxy-phenyl)-methanone(115969-26-1)
• EPA Substance Registry System: [2-Azepan-1-yl-4-(4-nitro-phenyl)-thiazol-5-yl]-(4-methoxy-phenyl)-methanone(115969-26-1)

Safety Data

• Hazardous Substances Data: 115969-26-1(Hazardous Substances Data)

Upstream product

• 5321-89-1 hexahydroazepin-1-yl cianide 
• 111-49-9 hexamethylene imine 
• 68881-66-3 1-thiocarbamoylhexahydroazepine 
• 99-81-0 4-Nitrophenacyl bromide 
• 114171-16-3 1-hexahydroazepine 

Relevant articles and documents

A Study of Three Reactions leading to Isomeric 2-(N,N-Disubstituted Amino)thiazol-5-yl Ketones

N-Imidoyl-N,N-disubstituted thioureas react with α-halogeno ketones in the presence of triethylamine to give the expected 2-(N,N-disubstituted amino)thiazol-5-yl ketones in high yield.The corresponding reactions of N-acyl-N,N-disubstituted thioureas lead

THE USE OF PROTIUM AND DEUTERIUM ANALOGUES IN MECHANISTIC STUDIES OF THIAZOLE SYNTHESES

The mechanism of two reactions which give isomeric thiazol-5-yl ketones have been elucidated by work with substrates containing pairs of acyl groups and their deuterium-substituted analogues.