Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)-

Base Information

Chemical Name:Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)-
CAS No.:135718-54-6
Molecular Formula:C₁₂H₉ClN₂S
Molecular Weight:248.736
Hs Code.:
DSSTox Substance ID:DTXSID20332911
Nikkaji Number:J407.106I
Wikidata:Q82097831
Mol file:135718-54-6.mol

Synonyms:135718-54-6;Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)-;2-chloro-6-(p-tolyl)imidazo[2,1-b]thiazole;DTXSID20332911;AKOS005144946;2-Chloro-6-(4-methylphenyl)imidazo[2,1-b]thiazole

Suppliers and Price of Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)-

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 Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)-

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:248.0174972
Heavy Atom Count:16
Complexity:255

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C2=CN3C=C(SC3=N2)Cl

Technology Process of Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)-

There total 1 articles about Imidazo[2,1-b]thiazole, 2-chloro-6-(4-methylphenyl)- 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:

: 41663-73-4
2-amino-5-chlorothiazole

: 619-41-0
4-(bromoacetyl)toluene

: 135718-54-6
2-Chloro-6-p-tolyl-imidazo[2,1-b]thiazole

Guidance literature:: With hydrogen bromide; Yield given. Multistep reaction; 1.) acetone, reflux, 3 h, 2.) reflux, 1 h;
DOI:10.1016/0223-5234(91)90067-W