1606142-35-1

Basic information

• Product Name: 4-(4-chlorophenyl)-2-(4-(N,N-dimethylamino)phenyl)-2,3-dihydro-1,5-benzothiazepine
• CAS NO: 1606142-35-1
• Molecular Weight: 392.952
• Mol File: 1606142-35-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-(4-chlorophenyl)-2-(4-(N,N-dimethylamino)phenyl)-2,3-dihydro-1,5-benzothiazepine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-chlorophenyl)-2-(4-(N,N-dimethylamino)phenyl)-2,3-dihydro-1,5-benzothiazepine(1606142-35-1)
• EPA Substance Registry System: 4-(4-chlorophenyl)-2-(4-(N,N-dimethylamino)phenyl)-2,3-dihydro-1,5-benzothiazepine(1606142-35-1)

Safety Data

• Hazardous Substances Data: 1606142-35-1(Hazardous Substances Data)

Upstream product

• 85460-66-8 4-dimethylaminobenzal-4'-chloroacetophenone 
• 137-07-5 2-amino-benzenethiol 
• 99-91-2 para-chloroacetophenone 
• 100-10-7 4-dimethylamino-benzaldehyde 

Relevant articles and documents

Ionic Liquid-Assisted Preparation of Co3O4 Nanosheets as a New and Efficient Catalyst for Green Synthesis of Various 1,5-Benothiazepine Derivatives in Water

Abstract: A novel and green method for the preparation of cobalt oxide nanosheets using pyridinium-based ionic liquid by simple reflux method is described in the present work. Pyridinium-based ionic liquid, N-butyl pyridinium bromide [BuPy]Br plays an important role as reaction media and morphology template to control Co3O4 nanostructures. This catalyst is characterized by XRD, FE-SEM, FT-IR, VSM and UV-Visible spectroscopy. Further, this nanocatalyst is used to catalyzes the condensation reaction of o-amino thiophenol with α,β-unsaturated ketones for preparation of 1,5-benzothiazepine derivatives in excellent yields. This efficient catalyst could be recovered and reused several times without any significant loss of activity.