N-Phenyl-N'-phenylsulfonylthiourea

Base Information

Chemical Name:N-Phenyl-N'-phenylsulfonylthiourea
CAS No.:24539-87-5
Molecular Formula:C13H12 N2 O2 S2
Molecular Weight:292.382
Hs Code.:2935009090
DSSTox Substance ID:DTXSID20947423
Nikkaji Number:J48.966B
Mol file:24539-87-5.mol

Synonyms:24539-87-5;N-Phenyl-N'-phenylsulfonylthiourea;n-(phenylcarbamothioyl)benzenesulfonamide;UREA, 1-PHENYL-3-(PHENYLSULFONYL)-2-THIO-;N-[Phenylamino(thioxo)methyl]benzenesulfonamide;1-(benzenesulfonyl)-3-phenylthiourea;Oprea1_691280;Benzenesulfonamide, N-[(phenylamino)thioxomethyl]-;DTXSID20947423;DQZVRFYALJGUCL-UHFFFAOYSA-N;AKOS002205457;N-Phenyl- N'-benzolsulfonylthioharnstoff;([(Anilinocarbothioyl)amino]sulfonyl)benzene #;N-(Benzenesulfonyl)-N'-phenylcarbamimidothioic acid;F1535-0003

Suppliers and Price of N-Phenyl-N'-phenylsulfonylthiourea

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
Packaging
price

Total 4 raw suppliers

Chemical Property of N-Phenyl-N'-phenylsulfonylthiourea

Chemical Property:

Vapor Pressure:3.98E-08mmHg at 25°C
Boiling Point:445.3°Cat760mmHg
Flash Point:223.1°C
PSA：98.67000
Density:1.399g/cm³
LogP:3.90660
XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:292.03401998
Heavy Atom Count:19
Complexity:391

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=S)NS(=O)(=O)C2=CC=CC=C2

Technology Process of N-Phenyl-N'-phenylsulfonylthiourea

There total 5 articles about N-Phenyl-N'-phenylsulfonylthiourea 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: 92.0%

: 1424-53-9
benzenesulfonyl isothiocyanate

: 62-53-3
aniline

: 24539-87-5
N-phenyl-N'-benzenesulphonylthiocarbamide

Guidance literature:: In benzene; at -5 ℃; for 2h;

Reference yield: 75.0%

: 98-10-2
benzenesulfonamide

: 103-72-0
phenyl isothiocyanate

: 24539-87-5
N-phenyl-N'-benzenesulphonylthiocarbamide

Guidance literature:: With potassium carbonate; In acetone; for 11h; Heating;

Reference yield:

: 18418-42-3
phenyl-dithiocarbamic acid; sodium salt

: 24539-87-5
N-phenyl-N'-benzenesulphonylthiocarbamide

Guidance literature:: Multi-step reaction with 2 steps

1: water

2: potassium hydroxide / water

With potassium hydroxide; In water;
DOI:10.3998/ark.5550190.0013.922