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1,5-Benzothiazepine

Base Information
  • Chemical Name:1,5-Benzothiazepine
  • CAS No.:265-13-4
  • Molecular Formula:C9H7 N S
  • Molecular Weight:161.22
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00604921
  • Nikkaji Number:J372.679G
1,5-Benzothiazepine

Synonyms:1,5-benzothiazepine

Suppliers and Price of 1,5-Benzothiazepine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of 1,5-Benzothiazepine
Chemical Property:
  • Boiling Point:270.7±40.0 °C(Predicted) 
  • PSA:37.66000 
  • Density:1.15±0.1 g/cm3(Predicted) 
  • LogP:2.44390 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:161.02992040
  • Heavy Atom Count:11
  • Complexity:186
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)N=CC=CS2
  • General Description 1,5-Benzothiazepine, also known as 1-Thia-5-azabenzocycloheptene, is a heterocyclic compound that can be synthesized efficiently under solvent-free conditions using chalcones and o-amino thiophenol with inorganic supports. 1,5-Benzothiazepine and its derivatives have been characterized spectroscopically and demonstrate weak to moderate antibacterial activity against certain pathogens, making them of potential interest in medicinal chemistry. The solvent-free synthesis method offers environmental and efficiency advantages over traditional approaches.
Refernces

Solvent-free synthesis of some 1,5-benzothiazepines and benzodiazepines and their antibacterial activity

10.1080/10426500701852661

The research focuses on an efficient and convenient method for synthesizing 1,5-benzothiazepines and benzodiazepines without the use of solvents. The study employs chalcones as starting materials, reacting them with o-amino thiophenol and o-phenylenediamine in the presence of inorganic supports such as silica gel and alumina. These reactions are carried out at 80°C under solvent-free conditions, resulting in the formation of the desired heterocyclic compounds. The synthesized compounds are characterized using elemental analysis, IR, 1H NMR, and 13C NMR spectroscopy. The research also evaluates the antibacterial activity of the synthesized compounds against pathogens like B. subtilis, E. coli, and S. typhi, revealing that some of the compounds exhibit weak to moderate antibacterial activity. The study highlights the advantages of solvent-free conditions over traditional methods, emphasizing the efficiency and environmental benefits of this approach in the synthesis of these important heterocyclic compounds.

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