6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime

Base Information

Chemical Name:6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime
CAS No.:23576-85-4
Molecular Formula:C₆H₄ClN₃OS
Molecular Weight:201.636
Hs Code.:2934100090
NSC Number:332734
Mol file:23576-85-4.mol

Synonyms:(E)-N-({6-chloroimidazo[2,1-b][1,3]thiazol-5-yl}methylidene)hydroxylamine;1056188-92-1;6-chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime;NSC332734;SCHEMBL5904879;HMS1364O19;AKOS008939645;NSC-332734;9D-074

Suppliers and Price of 6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime

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

American Custom Chemicals Corporation
6-CHLOROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBOXALDEHYDE OXIME 95.00%
5MG
$ 633.99

American Custom Chemicals Corporation
6-CHLOROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBOXALDEHYDE OXIME 95.00%
10MG
$ 631.85

American Custom Chemicals Corporation
6-CHLOROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBOXALDEHYDE OXIME 95.00%
1MG
$ 597.89

Total 6 raw suppliers

Chemical Property of 6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime

Chemical Property:

PSA：78.13000
Density:1.77g/cm³
LogP:1.85730
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:200.9763606
Heavy Atom Count:12
Complexity:203

Purity/Quality:

99% ^*data from raw suppliers

6-CHLOROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBOXALDEHYDE OXIME 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CSC2=NC(=C(N21)C=NO)Cl
Isomeric SMILES:C1=CSC2=NC(=C(N21)/C=N/O)Cl

Technology Process of 6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime

There total 3 articles about 6-Chloroimidazo[2,1-b][1,3]thiazole-5-carbaldehyde oxime 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:

: 23576-84-3
6-chloro-imidazo-[2,1-b]thiazole-5-carbaldehyde

: 23576-85-4
6-Chlorimidazo<2,1-b>thiazol-5-aldoxim

Guidance literature:: With ammonium hydroxide; hydroxylamine hydrochloride; In ethanol; water; for 0.166667h; pH=6; Reflux;
DOI:10.2174/1573406413666171010110819

Reference yield:

: 23576-81-0
6-chloroimidazo[2,1-b]thiazole

: 23576-85-4
6-Chlorimidazo<2,1-b>thiazol-5-aldoxim

Guidance literature:: Multi-step reaction with 2 steps

1.1: trichlorophosphate / chloroform / 0 - 5 °C

1.2: 5 h / Reflux

2.1: hydroxylamine hydrochloride; ammonium hydroxide / ethanol; water / 0.17 h / pH 6 / Reflux

With ammonium hydroxide; hydroxylamine hydrochloride; trichlorophosphate; In ethanol; chloroform; water;
DOI:10.2174/1573406413666171010110819