1,2-Dithiocane

Base Information

Chemical Name:1,2-Dithiocane
CAS No.:6008-69-1
Molecular Formula:C6H12S2
Molecular Weight:148.293
Hs Code.:

Synonyms:

Suppliers and Price of 1,2-Dithiocane

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 13 raw suppliers

Chemical Property of 1,2-Dithiocane

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Use Description 1,2-Dithiocane, a chemical compound, has applications across various fields. In the field of organic chemistry, it serves as a valuable starting material or reagent for the synthesis of complex organic molecules, potentially contributing to the development of pharmaceuticals, agrochemicals, and specialty chemicals due to its versatile structure. In the realm of materials science and polymer chemistry, 1,2-Dithiocane can be employed as a building block for the creation of specialized materials, such as polymers or coatings, with unique properties for applications ranging from electronics to catalysis. Additionally, in the field of coordination chemistry, 1,2-Dithiocane may find use as a ligand or chelating agent, forming stable complexes with metal ions, which have applications in catalysis, material synthesis, and analytical chemistry. Its adaptability as an intermediate, materials precursor, and chelating agent underscores its significance in advancing pharmaceuticals, materials science, and coordination chemistry in various fields.

Technology Process of 1,2-Dithiocane

There total 10 articles about 1,2-Dithiocane 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: 99.5%

: 1191-43-1
1,6-dimercaptohexane

: 6008-69-1
1,2-dithiacyclooctane

Guidance literature:: With dihydrogen peroxide; at 25 - 30 ℃; for 1.5h; Temperature;

Reference yield: 72.0%

: 155345-54-3
1-bromo-6-iodohexane

: 6008-69-1
1,2-dithiacyclooctane

Guidance literature:: With benzyltriethylammonium tetrathiomolybdate; In chloroform; at 28 ℃; for 3h;

Reference yield: 65.0%

: 1191-43-1
1,6-dimercaptohexane

: 6008-69-1
1,2-dithiacyclooctane

: 13375-94-5
1,2,9,10-tetrathiacyclohexadecane

Guidance literature:: With iodine; triethylamine; In chloroform; at 20 ℃; for 5h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.inorgchem.7b01398