4751-59-1

Basic information

• Product Name: 4H-Thieno[3,2-c]azepin-4-one, 5,6,7,8-tetrahydro-
• CAS NO: 4751-59-1
• Molecular Formula: C8H9NOS
• Molecular Weight: 167.22800
• Mol File: 4751-59-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 92-93 °C
• Boiling Point: 415.5±24.0 °C(Predicted)
• Density: 1.229±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4H-Thieno[3,2-c]azepin-4-one, 5,6,7,8-tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-Thieno[3,2-c]azepin-4-one, 5,6,7,8-tetrahydro-(4751-59-1)
• EPA Substance Registry System: 4H-Thieno[3,2-c]azepin-4-one, 5,6,7,8-tetrahydro-(4751-59-1)

Safety Data

• Hazardous Substances Data: 4751-59-1(Hazardous Substances Data)

Upstream product

• 19995-19-8 4,5,6,7-tetrahydro-4-oxobenzo[b]thiophene oxime 
• 859204-24-3 methyl 2-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate 
• 4651-81-4 Methyl 2-aminothiophene-3-carboxylate 
• 76360-43-5 methyl 2-bromothiophene-3-carboxylate 
• 24287-95-4 2-bromothiophene-3-carboxylic acid 
• 13414-95-4 4-keto-4,5,6,7-tetrahydrothianaphthene 

Relevant articles and documents

p-diaminobenzene derivative as potassium channel regulator, preparation method and medical applications thereof

The invention relates to a p-diaminobenzene derivative as a potassium channel regulator, a preparation method and medical applications thereof, and specifically discloses a compound represented by a general formula A or a pharmaceutically acceptable salt

Regioselective synthesis of several heterocyclic fused azepines using diisobutylaluminum hydride

5,6,7,8-Tetrahydrothieno[3,2-b]azepine,5,6,7,8-tetrahydro-1H-furo[3,2-b] azepine, and 1,4,5,6,7,8-hexahydropyrrolo[3,2-b]azepine were synthesized by the ring expansion reaction of heterocyclic fused cyclohexanone oximes with diisobutylaluminum hydride (DIBAH). The mechanism of the reaction was different from that of Beckmann rearrangement.