1260668-12-9

Basic information

• Product Name: 4-chloro-2-((E)-2-(4-fluorophenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4-yl)-5-methylphenol
• Synonyms: 4-chloro-2-((E)-2-(4-fluorophenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4-yl)-5-methylphenol
• CAS NO: 1260668-12-9
• Molecular Weight: 397.9
• Mol File: 1260668-12-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-chloro-2-((E)-2-(4-fluorophenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4-yl)-5-methylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-2-((E)-2-(4-fluorophenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4-yl)-5-methylphenol(1260668-12-9)
• EPA Substance Registry System: 4-chloro-2-((E)-2-(4-fluorophenyl)-2,3-dihydrobenzo[b][1,4]thiazepin-4-yl)-5-methylphenol(1260668-12-9)

Safety Data

• Hazardous Substances Data: 1260668-12-9(Hazardous Substances Data)

Upstream product

• 1260667-96-6 (E)-1-(5-chloro-2-hydroxy-4-methylphenyl)-3-(4-fluorophenyl)prop-2-en-1-one 
• 137-07-5 2-amino-benzenethiol 
• 28480-70-8 5'-chloro-2'-hydroxy-4'-methyl acetophenone 
• 459-57-4 4-fluorobenzaldehyde 
• 165612-80-6 C₁₆H₁₂ClFO₂ 

Relevant articles and documents

An improved procedure for the synthesis of 1,5-benzothiazepines using ceric ammonium nitrate (CAN)

A mild and efficient procedure for the synthesis of various 1,5-benzothiazepines were developed. This method provides an easy access for preparation of 1,5-benzothiazepine derivatives in the presence of 10 mol% catalyst of CAN under ultrasonic irradiation. This method provided clean conversion, mild reaction condition, no use of toxic solvent and shorter reaction time compared to other reported method. Copyright