p-Toluenesulfonamide, N-(4-chloro-3-oxobutyl)-

Base Information

Chemical Name:p-Toluenesulfonamide, N-(4-chloro-3-oxobutyl)-
CAS No.:31984-14-2
Molecular Formula:C11H14 Cl N O3 S
Molecular Weight:243.71
Hs Code.:
Mol file:31984-14-2.mol

Synonyms:p-Toluenesulfonamide,N-(4-chloro-3-oxobutyl)- (8CI); 4-Tosylamido-1-chloro-2-butanone

Suppliers and Price of p-Toluenesulfonamide, N-(4-chloro-3-oxobutyl)-

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

American Custom Chemicals Corporation
P-TOLUENESULFONAMIDE, N-(4-CHLORO-3-OXOBUTYL)- 95.00%
5MG
$ 501.53

Total 5 raw suppliers

Chemical Property of p-Toluenesulfonamide, N-(4-chloro-3-oxobutyl)-

Chemical Property:

Vapor Pressure:1.64E-07mmHg at 25°C
Refractive Index:1.5800 (estimate)
Boiling Point:427.5°Cat760mmHg
PKA:10.61±0.50(Predicted)
Flash Point:212.3°C
PSA：71.62000
Density:1.286g/cm³
LogP:2.94300

Purity/Quality:

99% ^*data from raw suppliers

P-TOLUENESULFONAMIDE, N-(4-CHLORO-3-OXOBUTYL)- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of p-Toluenesulfonamide, N-(4-chloro-3-oxobutyl)-

There total 2 articles about p-Toluenesulfonamide, N-(4-chloro-3-oxobutyl)- 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: 44.0%

: 32065-38-6
N-(4-diazo-3-oxo-butyl)-toluene-4-sulfonamide

: 31984-14-2
N-(4-Chloro-3-oxo-butyl)-4-methyl-benzenesulfonamide

Guidance literature:: With hydrogenchloride; at 0 - 20 ℃;
DOI:10.1021/jm00177a012

Reference yield:

: 61341-03-5
N-(toluene-4-sulfonyl)-β-alanyl chloride

: 31984-14-2
N-(4-Chloro-3-oxo-butyl)-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / diethyl ether; CHCl₃ / 0 - 20 °C

2: 44 percent / HCl / 0 - 20 °C

With hydrogenchloride; In diethyl ether; chloroform;
DOI:10.1021/jm00177a012