2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane

Base Information

Chemical Name:2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane
CAS No.:791-50-4
Molecular Formula:C6F12S2
Molecular Weight:364.179
Hs Code.:
NSC Number:359467
UNII:QCC36T3ZR9
DSSTox Substance ID:DTXSID00229537
Nikkaji Number:J87.563E
Wikidata:Q83109825
Mol file:791-50-4.mol

Synonyms:2,2,4,4-tetrakis(trifluoromethyl)-1,3-dithietane;791-50-4;2,2,4,4-Tetra(trifluoromethyl)-1,3-dithiacyclobutane;1,3-Dithietane, 2,2,4,4-tetrakis(trifluoromethyl)-;Hexafluorothioacetone dimer;BRN 1257024;QCC36T3ZR9;AI3-61955;1,3-DITHIACYCLOBUTANE, 2,2,4,4-TETRA(TRIFLUOROMETHYL)-;NSC-359467;tetrakis(trifluoromethyl)-1,3-dithietane;5-19-01-00089 (Beilstein Handbook Reference);NSC359467;UNII-QCC36T3ZR9;SCHEMBL4420545;C6F12S2;DTXSID00229537;C6-F12-S2;AKOS037621787;NSC 359467;LS-63097;CS-0236425;EN300-1709109

Suppliers and Price of 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane

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

TRC
2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane
5g
$ 1610.00

TRC
2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane
2.5g
$ 845.00

Total 10 raw suppliers

Chemical Property of 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane

Chemical Property:

Vapor Pressure:5.06mmHg at 25°C
Boiling Point:149.7°C at 760 mmHg
Flash Point:44.3°C
PSA：50.60000
Density:1.829g/cm³
LogP:5.10820
XLogP3:5.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:0
Exact Mass:363.9249803
Heavy Atom Count:20
Complexity:305

Purity/Quality:

99%, ^*data from raw suppliers

2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1(SC(S1)(C(F)(F)F)C(F)(F)F)(C(F)(F)F)C(F)(F)F
General Description 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane, also known as hexafluorothioacetone dimer, is a reactive cyclic sulfur-containing compound that participates in diverse transformations. It reacts with azoles to form N-(hexafluoro-isopropyl)azoles and sulfur, serves as a precursor for thietane derivatives via fluoride-catalyzed reactions with ketene acetals, and undergoes [2+2] cycloadditions with N-vinyl compounds to yield 4-amino-2,2-bis(trifluoromethyl)thietanes. Additionally, it can undergo ring-opening processes under certain conditions, demonstrating its versatility in generating fluorinated sulfur-containing structures.

Technology Process of 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane

There total 27 articles about 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane 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: 92.0%