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

Base Information

Chemical Name:N,4-Dimethyl-N-(5-phenyl-1,2,4-thiadiazol-3-YL)benzenesulfonamide
CAS No.:89879-97-0
Molecular Formula:C16H15N3O2S2
Molecular Weight:345.446
Hs Code.:
DSSTox Substance ID:DTXSID10520845
Wikidata:Q82384981

Synonyms:89879-97-0;N,4-DIMETHYL-N-(5-PHENYL-1,2,4-THIADIAZOL-3-YL)BENZENESULFONAMIDE;DTXSID10520845;N,4-Dimethyl-N-(5-phenyl-1,2,4-thiadiazol-3-yl)benzene-1-sulfonamide

Suppliers and Price of N,4-Dimethyl-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

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

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:345.06056908
Heavy Atom Count:23
Complexity:480

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)N(C)C2=NSC(=N2)C3=CC=CC=C3

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

There total 4 articles about N,4-Dimethyl-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: 93.0%

: 98-59-9
p-toluenesulfonyl chloride

: 27182-64-5
3-methylamino-5-phenyl-1,2,4-thiadiazole

: 89879-97-0
3--5-phenyl-1,2,4-thiadiazole

Guidance literature:: With pyridine; at 100 ℃; for 18.5h;

Reference yield:

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

: 89879-97-0
3--5-phenyl-1,2,4-thiadiazole

Guidance literature:: Multi-step reaction with 3 steps

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

2: 19 percent / hydrochloric acid / ethanol / 77 h / Heating

3: 93 percent / pyridine / 18.5 h / 100 °C

With pyridine; hydrogenchloride; sodium carbonate; In ethanol; chloroform;

Reference yield:

: 89879-99-2
N-(p-tolylsulphonyl)-2-methyl-5-phenyl-1,2,4-thiadiazol-3(2H)-imine

: 89879-97-0
3--5-phenyl-1,2,4-thiadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 19 percent / hydrochloric acid / ethanol / 77 h / Heating

2: 93 percent / pyridine / 18.5 h / 100 °C

With pyridine; hydrogenchloride; In ethanol;