N-benzothiazol-2-ylsulfanyl-N-methyl-benzothiazole-2-sulfenamide

Base Information

Chemical Name:N-benzothiazol-2-ylsulfanyl-N-methyl-benzothiazole-2-sulfenamide
CAS No.:24345-92-4
Molecular Formula:C₁₅H₁₁N₃S₄
Molecular Weight:361.536
Hs Code.:2934999090
Mol file:24345-92-4.mol

Synonyms:Di(2-benzothiazolesulfen)amide,N-methyl- (6CI,8CI); N-Methylbis(2-benzothiazolesulfen)amide; NSC 19641

Suppliers and Price of N-benzothiazol-2-ylsulfanyl-N-methyl-benzothiazole-2-sulfenamide

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-benzothiazol-2-ylsulfanyl-N-methyl-benzothiazole-2-sulfenamide

Chemical Property:

Vapor Pressure:1.59E-11mmHg at 25°C
Boiling Point:535.1°Cat760mmHg
Flash Point:277.4°C
PSA：136.10000
Density:1.54g/cm³
LogP:5.55220

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-benzothiazol-2-ylsulfanyl-N-methyl-benzothiazole-2-sulfenamide

There total 2 articles about N-benzothiazol-2-ylsulfanyl-N-methyl-benzothiazole-2-sulfenamide 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:

: 33405-92-4
2-benzothiazolylsulfenyl chloride

: 74-89-5
methylamine

: 24345-92-4
bis-(benzothiazole-2-sulfenyl)-methyl-amine

Guidance literature:: With benzene;

Reference yield:

: 120-78-5
di(benzothiazol-2-yl)disulfide

: 24345-92-4
bis-(benzothiazole-2-sulfenyl)-methyl-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 1,2-dichloro-ethane; chlorine

2: 1,2-dichloro-ethane

With chlorine; 1,2-dichloro-ethane;
DOI:10.1021/ie50603a031