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N-Benzylbenzenecarbothioamide

Base Information Edit
  • Chemical Name:N-Benzylbenzenecarbothioamide
  • CAS No.:14309-89-8
  • Molecular Formula:C14H13 N S
  • Molecular Weight:227.33
  • Hs Code.:
  • NSC Number:28119
  • DSSTox Substance ID:DTXSID80364334
  • Nikkaji Number:J362.315G
  • ChEMBL ID:CHEMBL4064333
  • Mol file:14309-89-8.mol
N-Benzylbenzenecarbothioamide

Synonyms:N-Benzylbenzenecarbothioamide;14309-89-8;NSC28119;N-Benzylbenzothioamide;N-benzyl(thiobenzamide);SCHEMBL1520880;CHEMBL4064333;SCHEMBL12045978;DTXSID80364334;NSC-28119;AKOS000346999;Benzenecarbothioamide, N-(phenylmethyl)-;SR-01000061402;SR-01000061402-1;Z48888792

Suppliers and Price of N-Benzylbenzenecarbothioamide
Supply Marketing:Edit
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 4 raw suppliers
Chemical Property of N-Benzylbenzenecarbothioamide Edit
Chemical Property:
  • Vapor Pressure:2.25E-05mmHg at 25°C 
  • Boiling Point:360.2°C at 760 mmHg 
  • Flash Point:171.6°C 
  • Density:1.146g/cm3 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:227.07687059
  • Heavy Atom Count:16
  • Complexity:215
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CNC(=S)C2=CC=CC=C2
Technology Process of N-Benzylbenzenecarbothioamide

There total 56 articles about N-Benzylbenzenecarbothioamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sulfur; In neat (no solvent); at 120 ℃; for 8h; Temperature; Inert atmosphere;
DOI:10.1021/ol302856w
Guidance literature:
With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1021/jo050670t
Guidance literature:
With sulfur; dimethyl sulfoxide; at 80 ℃; for 16h; Inert atmosphere;
DOI:10.1002/adsc.201801695
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