N-(4-Chlorophenyl)benzenesulfinamide

Base Information

Chemical Name:N-(4-Chlorophenyl)benzenesulfinamide
CAS No.:14934-02-2
Molecular Formula:C₁₂H₁₀ClNOS
Molecular Weight:251.737
Hs Code.:
NSC Number:95812
DSSTox Substance ID:DTXSID40294320
Nikkaji Number:J1.118.560F
Mol file:14934-02-2.mol

Synonyms:14934-02-2;N-(4-Chlorophenyl)benzenesulfinamide;NSC95812;DTXSID40294320;JPPSAQZNPMSNRP-UHFFFAOYSA-N;NSC-95812;AKOS002844443;N-(4-Chlorophenyl)benzenesulfinamide #;N-(p-Chlorophenyl)-benzenesulfinylamide

Suppliers and Price of N-(4-Chlorophenyl)benzenesulfinamide

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 6 raw suppliers

Chemical Property of N-(4-Chlorophenyl)benzenesulfinamide

Chemical Property:

Vapor Pressure:8.13E-07mmHg at 25°C
Boiling Point:406.5°Cat760mmHg
Flash Point:199.6°C
Density:1.39g/cm³
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:251.0171628
Heavy Atom Count:16
Complexity:235

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)S(=O)NC2=CC=C(C=C2)Cl

Technology Process of N-(4-Chlorophenyl)benzenesulfinamide

There total 5 articles about N-(4-Chlorophenyl)benzenesulfinamide 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:

: 618-41-7
Benzenesulfinic acid

: 14934-02-2
N-(4-Chlorophenyl)benzenesulfinamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride

2: diethyl ether

With thionyl chloride; diethyl ether;
DOI:10.1021/ja01314a038

Reference yield:

: 4972-29-6
benzenesulphinyl chloride

: 106-47-8
4-chloro-aniline

: 14934-02-2
N-(4-Chlorophenyl)benzenesulfinamide

Guidance literature:: With diethyl ether;
DOI:10.1021/ja01314a038

Reference yield:

: 108-98-5
thiophenol

: 14934-02-2
N-(4-Chlorophenyl)benzenesulfinamide

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuryl chloride / 0.05 h / 0 °C / 15 Torr

2: Et₃N / CH₂Cl₂ / 3 h / 0 °C

3: 1.) LDA, 2.) O₂ / 1.) THF, RT, 4 h, 2.) THF, RT, 20 h

With sulfuryl dichloride; oxygen; triethylamine; lithium diisopropyl amide; In dichloromethane;
DOI:10.1016/0040-4020(96)00799-5