N-(phenylsulfamoyl)aniline

Base Information Edit

Chemical Name:N-(phenylsulfamoyl)aniline
CAS No.:587-14-4
Molecular Formula:C12H12N2O2S
Molecular Weight:248.305
Hs Code.:
Nikkaji Number:J6.740G
Mol file:587-14-4.mol

Synonyms:SCHEMBL59151;AS-83187;E77709

Suppliers and Price of N-(phenylsulfamoyl)aniline

Supply Marketing:Edit

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

American Custom Chemicals Corporation
N,N'-DIPHENYLSULFAMIDE 95.00%
5MG
$ 497.22

Total 1 raw suppliers

Chemical Property of N-(phenylsulfamoyl)aniline Edit

Chemical Property:

Vapor Pressure:3.61E-07mmHg at 25°C
Melting Point:114 °C
Boiling Point:417.2°C at 760 mmHg
PKA:5.66±0.48(Predicted)
Flash Point:206.1°C
PSA：71.78000
Density:1.362g/cm³
LogP:3.80930
XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:248.06194880
Heavy Atom Count:17
Complexity:286

Purity/Quality:

99% ^*data from raw suppliers

N,N'-DIPHENYLSULFAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NS(=O)(=O)NC2=CC=CC=C2

Technology Process of N-(phenylsulfamoyl)aniline

There total 13 articles about N-(phenylsulfamoyl)aniline 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: 89.0%

: 62-53-3
aniline

: 587-14-4
N,N'-diphenylsulfamide

Guidance literature:: With sulfuryl dichloride; In neat (no solvent); for 0.583333h; Sonication; Green chemistry;
DOI:10.1080/10426507.2017.1287184