Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)-

Base Information

Chemical Name:Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)-
CAS No.:103503-25-9
Molecular Formula:C12H9N3O2S
Molecular Weight:259.288
Hs Code.:
DSSTox Substance ID:DTXSID10398001
Wikidata:Q82199700
Mol file:103503-25-9.mol

Synonyms:103503-25-9;3-Methyl-6-(4-nitrophenyl)imidazo[2,1-b]thiazole;Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)-;3-methyl-6-(4-nitrophenyl)imidazo[2,1-b][1,3]thiazole;SCHEMBL2193954;DTXSID10398001;UZZMSDAZUUEXEY-UHFFFAOYSA-N;AKOS001049737;SR-01000048902;SR-01000048902-1;Z56957541

Suppliers and Price of Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)-

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
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Total 0 raw suppliers

Chemical Property of Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)-

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:259.04154771
Heavy Atom Count:18
Complexity:328

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CSC2=NC(=CN12)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)-

There total 5 articles about Imidazo[2,1-b]thiazole, 3-methyl-6-(4-nitrophenyl)- 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: 77.0%

: 3-methyl-6-p-nitrophenyl-7H-imidazo<2,1-b>thiazolium bromide

: 103503-25-9
3-methyl-6-p-nitrophenylimidazo<2,1-b>thiazole

Guidance literature:: With sodium carbonate; In water;

Reference yield: 50.0%

: 1603-91-4
4-methylthiazol-2-ylamine

: 99-81-0
4-Nitrophenacyl bromide

: 103503-25-9
3-methyl-6-p-nitrophenylimidazo<2,1-b>thiazole

Guidance literature:: In ethanol; for 16h; Reflux;

Reference yield:

: 99-81-0
4-Nitrophenacyl bromide

: 103503-25-9
3-methyl-6-p-nitrophenylimidazo<2,1-b>thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / ethanol / 6 h / Heating

2: 77 percent / sodium carbonate / H₂O

With sodium carbonate; In ethanol; water;