N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine

Base Information

Chemical Name:N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine
CAS No.:89563-51-9
Molecular Formula:C₁₂H₁₃N₃O₂S
Molecular Weight:263.32
Hs Code.:
DSSTox Substance ID:DTXSID60521766
Wikidata:Q82386439

Synonyms:89563-51-9;N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine;DTXSID60521766

Suppliers and Price of N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:263.07284784
Heavy Atom Count:18
Complexity:292

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(SC(=N1)N(C)CC2=CC=CC=C2)[N+](=O)[O-]

Technology Process of N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine

There total 3 articles about N-Benzyl-N,4-dimethyl-5-nitro-1,3-thiazol-2-amine 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:

: 34065-04-8
N-benzyl-N-methyl cyanamide

: 89563-51-9
2-(N-benzyl-N-methylamino)-4-methyl-5-nitrothiazole

Guidance literature:: Multi-step reaction with 2 steps

1: H₂S, Et₃N / ethanol / 10 °C

2: 0.45 g / acetone / Heating

With hydrogen sulfide; triethylamine; In ethanol; acetone;
DOI:10.1039/P19840000147

Reference yield:

: 103-67-3
benzyl-methyl-amine

: 89563-51-9
2-(N-benzyl-N-methylamino)-4-methyl-5-nitrothiazole

Guidance literature:: Multi-step reaction with 3 steps

1: MgCO₃ / H₂O; diethyl ether / 5 °C

2: H₂S, Et₃N / ethanol / 10 °C

3: 0.45 g / acetone / Heating

With hydrogen sulfide; triethylamine; magnesium carbonate; In diethyl ether; ethanol; water; acetone;
DOI:10.1039/P19840000147