2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide

Base Information

Chemical Name:2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide
CAS No.:67024-10-6
Molecular Formula:C₁₀H₉ClN₂OS
Molecular Weight:240.713
Hs Code.:
DSSTox Substance ID:DTXSID10368744
Wikidata:Q82155530
ChEMBL ID:CHEMBL1302926

Synonyms:2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide;67024-10-6;STK355711;HMS2817O11;2-Chloro-N-(4,5-dihydro-thiazol-2-yl)-benzamide;MLS001208842;Benzamide, 2-chloro-N-(4,5-dihydro-2-thiazolyl)-;CHEMBL1302926;SCHEMBL11349130;DTXSID10368744;2-(2-chlorobenzoyl)iminothiazolidine;AKOS000462768;WAY-616463;SMR000523821;AK-968/40063220;SR-01000045253;SR-01000045253-1;Z30009085

Suppliers and Price of 2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide

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 1 raw suppliers

Chemical Property of 2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:240.0124118
Heavy Atom Count:15
Complexity:283

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CSC(=N1)NC(=O)C2=CC=CC=C2Cl

Technology Process of 2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide

There total 6 articles about 2-chloro-N-(4,5-dihydro-1,3-thiazol-2-yl)benzamide 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: 55.0%

: 151-56-4,9002-98-6
ethyleneimine

: 7047-16-7
(2-chloro-benzoyl)-dithiocarbamic acid methyl ester

: 67024-10-6
2-chloro-N-(4,5-dihydro-thiazol-2-yl)-benzamide

Guidance literature:: In diethyl ether; for 2h; Ambient temperature;

Reference yield:

: 156-57-0
2-mercaptoethylamine hydrochloride

: 74074-22-9
N-(Bis-methylsulfanyl-methylene)-2-chloro-benzamide

: 67024-10-6
2-chloro-N-(4,5-dihydro-thiazol-2-yl)-benzamide

Guidance literature:: With TEA; In ethanol; for 6h; Heating;

Reference yield:

: 609-65-4
o-chlorobenzoyl chloride

: 67024-10-6
(chloro-2' benzoyl) amino-2-Δ²-thiazoline

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 1 h / Heating

2: acetone / 2 h / Heating

In acetone;
DOI:10.1080/00397919108016753