N,N-Diethylbenzenesulfonamide

Base Information

Chemical Name:N,N-Diethylbenzenesulfonamide
CAS No.:1709-50-8
Molecular Formula:C10H15 N O2 S
Molecular Weight:213.301
Hs Code.:2935009090
NSC Number:3551
UNII:A6LR4L2AD6
DSSTox Substance ID:DTXSID8075120
Nikkaji Number:J41.396H
Wikidata:Q82003149
Mol file:1709-50-8.mol

Synonyms:N,N-diethylbenzenesulfonamide

Suppliers and Price of N,N-Diethylbenzenesulfonamide

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 11 raw suppliers

Chemical Property of N,N-Diethylbenzenesulfonamide

Chemical Property:

Vapor Pressure:0.000462mmHg at 25°C
Melting Point:38.5-40 °C(Solv: ethyl ether (60-29-7); hexane (110-54-3))
Refractive Index:1.5060 (estimate)
Boiling Point:314.6°C at 760 mmHg
PKA:-4.91±0.70(Predicted)
Flash Point:144°C
PSA：45.76000
Density:1.134g/cm³
LogP:2.79790
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:213.08234989
Heavy Atom Count:14
Complexity:246

Purity/Quality:: 99.5% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)S(=O)(=O)C1=CC=CC=C1

Technology Process of N,N-Diethylbenzenesulfonamide

There total 42 articles about N,N-Diethylbenzenesulfonamide 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: 97.0%

: 108-98-5
thiophenol

: 109-89-7
diethylamine

: 1709-50-8
N,N-diethylbenzenesulfonamide

Guidance literature:: thiophenol; With dihydrogen peroxide; zirconium(IV) chloride; In acetonitrile; at 25 ℃;

diethylamine; With pyridine; In acetonitrile; at 25 ℃; for 0.05h; chemoselective reaction;
DOI:10.1016/j.tetlet.2010.07.056