Disulfide, dichlorofluoromethyl trifluoromethyl

Base Information

• Chemical Name: Disulfide, dichlorofluoromethyl trifluoromethyl
• CAS No.: 20614-29-3
• Molecular Formula: C2Cl2F4S2
• Molecular Weight: 235.054

Synonyms:Disulfide,dichlorofluoromethyl trifluoromethyl;trifluoromethyl-dichlorofluoromethyldisulfane;Dichlorofluoromethyl trifluoromethyl disulfide;Trifluormethyl-dichlorfluormethyldisulfan;

Chemical Property of Disulfide, dichlorofluoromethyl trifluoromethyl

Chemical Property:

• Boiling Point: 93.6±40.0 °C(Predicted)
• PSA: 50.60000
• Density: 1.752±0.06 g/cm3(Predicted)
• LogP: 3.94600

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Disulfide, dichlorofluoromethyl trifluoromethyl

There total 2 articles about Disulfide, dichlorofluoromethyl trifluoromethyl 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:

Trifluoromethylsulfenyl chloride (421-17-0) → Bis(trifluoromethyl)disulfid (372-64-5) + trifluoromethyl-dichlorofluoromethyldisulfane (20614-29-3) + bis(trifluoromethylthio)selenide

Guidance literature:

With dmap; hydrogen selenide; at -78 ℃; for 3h; Product distribution;

DOI:10.1016/0022-1139(93)02928-8

Reference yield:

Trifluoromethylsulfenyl chloride (421-17-0) → Bis(trifluoromethyl)disulfid (372-64-5) + bis(trifluoromethyl)trisulfide (372-06-5) + bis(trifluoromethyl)tetrasulfide (372-07-6) + trifluoromethyl-dichlorofluoromethyldisulfane (20614-29-3) + bis(trifluoromethyl)pentasulfide

Guidance literature:

With dmap; hydrogen sulfide; at -78 ℃; for 3h; Product distribution; Mechanism;

DOI:10.1016/0022-1139(93)02928-8

upstream raw materials:

Trifluoromethylsulfenyl chloride

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