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Trifluoromethyl(pentafluoroethyl)sulfane, also known as 1,1,2,2,3,3-hexafluoropropyl methyl sulfide, is a colorless, volatile, and highly reactive organosulfur compound with the chemical formula C3F6S. It consists of a sulfur atom bonded to a trifluoromethyl group (CF3) and a pentafluoroethyl group (CF2CF2CF3). trifluoromethyl(pentafluoroethyl)sulfane is an important intermediate in the synthesis of various fluorinated compounds, particularly those used in pharmaceuticals, agrochemicals, and specialty materials. Due to its high reactivity and sensitivity to moisture and air, it is typically handled under anhydrous and anaerobic conditions. Trifluoromethyl(pentafluoroethyl)sulfane is also known for its potential use as a precursor in the preparation of fluorinated heterocycles and other complex molecules.

33547-10-3

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33547-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33547-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33547-10:
(7*3)+(6*3)+(5*5)+(4*4)+(3*7)+(2*1)+(1*0)=103
103 % 10 = 3
So 33547-10-3 is a valid CAS Registry Number.

33547-10-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trifluoromethyl(pentafluoroethyl)sulfane

1.2 Other means of identification

Product number -
Other names Pentafluorethyl-trifluormethyl-sulfid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33547-10-3 SDS

33547-10-3Downstream Products

33547-10-3Relevant academic research and scientific papers

Reactions of the difluoramine-potassium fluoride adduct, HNF2·KF, with sulfinyl and perfluoroalkylsulfinyl fluorides. Preparation of perfluoroalkyl perfluoroalkylthiosulfonates

De Marco, Ronald A.,Shreeve, Jean'ne M.

, p. 1896 - 1899 (2007/10/12)

The reaction of HNF2·KF with sulfinyl fluoride gave FS(O)NF2 which was isolated and had sufficient stability to be characterized by spectroscopic methods. Attempts to prepare CF3S(O)NF2 and C2F5S(O)NF2 resulted in the formation of N2F4 and the perfluoroalkyl perfluoroalkylthiosulfonate esters CF3SO2SCF3 and C2F5SO2C2F5. Efforts to synthesize additional thiosulfonate esters led to the characterization of C2F5S(O)Cl, 19F nmr spectral identification of C2F5SO2SCF3 and CF3SO2SC2F5, and spectroscopic characterization of the previously reported C2F5SO2F.

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