N-benzoyl-N'-(8-quinolinyl)thiourea

Base Information

Chemical Name:N-benzoyl-N'-(8-quinolinyl)thiourea
CAS No.:130818-06-3
Molecular Formula:C17H13N3OS
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID90393731
Wikidata:Q82192632
ChEMBL ID:CHEMBL1481343

Synonyms:130818-06-3;N-benzoyl-N'-(8-quinolinyl)thiourea;N-(quinolin-8-ylcarbamothioyl)benzamide;Benzamide, N-[(8-quinolinylamino)thioxomethyl]-;HMS2187L09;SMR000179258;MLS000326723;CHEMBL1481343;SCHEMBL12747952;DTXSID90393731;MFCD01568682;1-benzoyl-3-(quinolin-8-yl)thiourea;AKOS005096408;6N-056;PHENYL-N-((8-QUINOLYLAMINO)THIOXOMETHYL)FORMAMIDE

Suppliers and Price of N-benzoyl-N'-(8-quinolinyl)thiourea

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 4 raw suppliers

Chemical Property of N-benzoyl-N'-(8-quinolinyl)thiourea

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:307.07793322
Heavy Atom Count:22
Complexity:409

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC(=S)NC2=CC=CC3=C2N=CC=C3

Technology Process of N-benzoyl-N'-(8-quinolinyl)thiourea

There total 2 articles about N-benzoyl-N'-(8-quinolinyl)thiourea 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:

Reference yield:

: 98-88-4
benzoyl chloride

: 130818-06-3
1-benzoyl-3-(quinolin-8-yl)thiourea

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 1 h / Reflux

2: acetone / 2 h / 20 °C / Reflux

In acetone;
DOI:10.1016/j.molstruc.2019.02.098