2,6-Dichloroimidazo[2,1-b][1,3]thiazole

Base Information

Chemical Name:2,6-Dichloroimidazo[2,1-b][1,3]thiazole
CAS No.:135718-53-5
Molecular Formula:C₅H₂Cl₂N₂S
Molecular Weight:193.056
Hs Code.:2934100090
DSSTox Substance ID:DTXSID80577129
Nikkaji Number:J407.105K
Wikidata:Q82467057
Mol file:135718-53-5.mol

Synonyms:2,6-Dichloroimidazo[2,1-b]thiazole;135718-53-5;2,6-dichloroimidazo[2,1-b][1,3]thiazole;Imidazo[2,1-b]thiazole, 2,6-dichloro-;SCHEMBL1665689;DTXSID80577129;PHGWIAWEBQAWJE-UHFFFAOYSA-N;AKOS006314527;AT35321;BS-50023;CS-0199309

Suppliers and Price of 2,6-Dichloroimidazo[2,1-b][1,3]thiazole

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

Crysdot
2,6-Dichloroimidazo[2,1-b]thiazole 95+%
1g
$ 772.00

American Custom Chemicals Corporation
2,6-DICHLOROIMIDAZO[2,1-B]THIAZOLE 95.00%
5MG
$ 500.58

Alichem
2,6-Dichloroimidazo[2,1-b]thiazole
1g
$ 659.40

AccelPharmtech
2,6-dichloroimidazo[2,1-b]thiazole 97.00%
25G
$ 4010.00

AccelPharmtech
2,6-dichloroimidazo[2,1-b]thiazole 97.00%
5G
$ 2180.00

AccelPharmtech
2,6-dichloroimidazo[2,1-b]thiazole 97.00%
1G
$ 1940.00

Total 8 raw suppliers

Chemical Property of 2,6-Dichloroimidazo[2,1-b][1,3]thiazole

Chemical Property:

PSA：45.54000
Density:1.848g/cm3
LogP:2.70260
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:191.9315746
Heavy Atom Count:10
Complexity:146

Purity/Quality:

98%min ^*data from raw suppliers

2,6-Dichloroimidazo[2,1-b]thiazole 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(N=C2N1C=C(S2)Cl)Cl

Technology Process of 2,6-Dichloroimidazo[2,1-b][1,3]thiazole

There total 2 articles about 2,6-Dichloroimidazo[2,1-b][1,3]thiazole 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: 85.0%

: 916258-32-7
(5-chloro-2-imino-1,3-thiazol-3(2H)-yl)acetic acid hydrobromide

: 135718-53-5
2,6-dichloroimidazo[2,1-b][1,3]thiazole

Guidance literature:: With N,N-diethylaniline; trichlorophosphate; In toluene; for 3h; Heating / reflux;

Reference yield:

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

: 79-08-3
bromoacetic acid

: 135718-53-5
2,6-dichloroimidazo[2,1-b][1,3]thiazole

Guidance literature:: With trichlorophosphate; Yield given. Multistep reaction; 1.) EtOH, reflux, 6 h, 2.) reflux, 3 h;
DOI:10.1016/0223-5234(91)90067-W