4-[(4-Chloro-1,3-thiazol-2-yl)amino]benzenesulfonamide

Base Information

Chemical Name:4-[(4-Chloro-1,3-thiazol-2-yl)amino]benzenesulfonamide
CAS No.:912969-60-9
Molecular Formula:C₉H₈ClN₃O₂S₂
Molecular Weight:289.766
Hs Code.:
DSSTox Substance ID:DTXSID401232470

Synonyms:912969-60-9;DTXSID401232470;4-[(4-Chloro-2-thiazolyl)amino]benzenesulfonamide

Suppliers and Price of 4-[(4-Chloro-1,3-thiazol-2-yl)amino]benzenesulfonamide

Supply Marketing:

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

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Chemical Property of 4-[(4-Chloro-1,3-thiazol-2-yl)amino]benzenesulfonamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:288.9746465
Heavy Atom Count:17
Complexity:352

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1NC2=NC(=CS2)Cl)S(=O)(=O)N

Technology Process of 4-[(4-Chloro-1,3-thiazol-2-yl)amino]benzenesulfonamide

There total 4 articles about 4-[(4-Chloro-1,3-thiazol-2-yl)amino]benzenesulfonamide 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: 66.0%

: 81059-98-5
2-(4-sulphonamidophenyl)-amino-Δ²-thiazolin-4-one

: 912969-60-9
4-(4-chlorothiazol-2-ylamino)benzenesulfonamide

Guidance literature:: With tetrabutylammomium bromide; 2,3-Dimethylaniline; trichlorophosphate; In acetonitrile; at 80 ℃; for 5h;
DOI:10.1021/jm060545p

Reference yield:

: 63-74-1
sulfanilamide

: 912969-60-9
4-(4-chlorothiazol-2-ylamino)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / dioxane / Heating

2: 66 percent / tetrabutylammonium bromide; dimethylaniline; POCl₃ / acetonitrile / 5 h / 80 °C

With tetrabutylammomium bromide; 2,3-Dimethylaniline; trichlorophosphate; In 1,4-dioxane; acetonitrile;
DOI:10.1021/jm060545p

Reference yield:

: 63-74-1
sulfanilamide

: 912969-60-9
4-(4-chlorothiazol-2-ylamino)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-dimethyl-formamide / 2 h / 20 °C

2: ethanol / 1 h / Reflux

3: trichlorophosphate; pyridine / 3 h / Reflux

With pyridine; trichlorophosphate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2016.05.016