4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)benzenesulfonamide

Base Information

Chemical Name:4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)benzenesulfonamide
CAS No.:89879-96-9
Molecular Formula:C15H13N3O2S2
Molecular Weight:331.419
Hs Code.:
DSSTox Substance ID:DTXSID50520844
Wikidata:Q82384980

Synonyms:89879-96-9;4-METHYL-N-(5-PHENYL-1,2,4-THIADIAZOL-3-YL)BENZENESULFONAMIDE;DTXSID50520844;4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-yl)benzene-1-sulfonamide

Suppliers and Price of 4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)benzenesulfonamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)benzenesulfonamide

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:331.04491901
Heavy Atom Count:22
Complexity:452

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC2=NSC(=N2)C3=CC=CC=C3

Technology Process of 4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)benzenesulfonamide

There total 1 articles about 4-Methyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)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: 28.0%

: 27182-54-3
5-phenyl-1,2,4-thiadiazol-3-amine

: 98-59-9
p-toluenesulfonyl chloride

: 89879-96-9
5-phenyl-3-(toluene-p-sulphonamido)-1,2,4-thiadiazole

: 89879-95-8
5-phenyl-3--1,2,4-thiadiazole

Guidance literature:: With pyridine; at 100 ℃; for 4h;

Reference yield:

: 89879-96-9
5-phenyl-3-(toluene-p-sulphonamido)-1,2,4-thiadiazole

: 65-85-0,8013-63-6
benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 41 percent / sodium carbonate / CHCl₃ / 28 h / Heating

2: potassium carbonate, water / ethanol / 0.04 h / 100 °C

With water; sodium carbonate; potassium carbonate; In ethanol; chloroform;

Reference yield:

: 89879-96-9
5-phenyl-3-(toluene-p-sulphonamido)-1,2,4-thiadiazole

: 89880-00-2
N-benzoyl-N'-methyl-N''-(p-tolylsulphonyl)guanidine

Guidance literature:: Multi-step reaction with 2 steps

1: 41 percent / sodium carbonate / CHCl₃ / 28 h / Heating

2: potassium carbonate, water / ethanol / 0.04 h / 100 °C

With water; sodium carbonate; potassium carbonate; In ethanol; chloroform;