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371-78-8

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371-78-8 Usage

Description

Bis(trifluoromethyl)sulfide, also known as trifluoromethyl disulfide, is a chemical compound with the molecular formula (CF3)2S. It is a colorless, flammable liquid with a pungent odor and is highly reactive, acting as a sulfenylating agent that can transfer its sulfur atom to other molecules. bis(trifluoromethyl)sulfide is used as a solvent and reagent in organic synthesis and has potential applications in the pharmaceutical and agrochemical industries due to its unique chemical properties.

Uses

Used in Organic Synthesis:
Bis(trifluoromethyl)sulfide is used as a solvent and reagent in organic synthesis for its ability to transfer its sulfur atom to other molecules, making it a valuable component in the creation of various chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, bis(trifluoromethyl)sulfide is used as a reagent for the synthesis of drug molecules, leveraging its unique chemical properties to create new and effective medications.
Used in Agrochemical Industry:
Bis(trifluoromethyl)sulfide also has potential applications in the agrochemical industry, where it can be utilized in the development of pesticides and other agricultural chemicals, contributing to enhanced crop protection and yield.
However, it is crucial to handle bis(trifluoromethyl)sulfide with care due to its toxicity and potential to cause irritation to the respiratory system, skin, and eyes. Proper safety measures should be taken to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 371-78-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 371-78:
(5*3)+(4*7)+(3*1)+(2*7)+(1*8)=68
68 % 10 = 8
So 371-78-8 is a valid CAS Registry Number.
InChI:InChI=1/C2F6S/c3-1(4,5)9-2(6,7)8

371-78-8SDS

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 trifluoro(trifluoromethylsulfanyl)methane

1.2 Other means of identification

Product number -
Other names Methane, thiobis[trifluoro-

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:371-78-8 SDS

371-78-8Relevant articles and documents

BEITRAEGE ZUR CHEMIE DER SCHEFELHALOGENIDE 15. DICHLOR-FLUOR-TRIFLUOROMETHYLSULFURAN, CF3SCl2F

Minkwitz, Rolf,Nass, Ulrike

, p. 393 - 398 (1987)

The preparation of the sulfurane CF3SCl2F is reported.Upon sublimation of the sulfonium salt CF3SCl2+AsF6- the compounds CF3SCl2F and AsF5 coexist in the gaseous phase.After trapping AsF5 as KAsF6 extremely instable CF3SCl2F is isolated and characterised by IR-, Raman- and 19F-NMR-spectroscopy.

Copper(I)-mediated direct trifluoromethylthiolation of allylic halides with elemental sulfur and (trifluoromethyl)trimethylsilane

Li, Jue,Wang, Peiqiang,Xie, Fei-Fei,Yang, Xi-Gang,Song, Xiao-Nan,Chen, Wei-Dong,Ren, Jiangmeng,Zeng, Bu-Bing

supporting information, p. 3568 - 3571 (2015/06/08)

Abstract A new method has been developed for the copper-mediated trifluoromethylthiolation of allylic halides by using potassium fluoride, elemental sulfur, and (trifluoromethyl)trimethylsilane in anhydrous N,N-dimethylformamide. This protocol provides facile access to a variety of allylic trifluoromethyl thioethers in moderate to good yields under mild, ligand-free reaction conditions.

GASEOUS DIELECTRICS WITH LOW GLOBAL WARMING POTENTIALS

-

, (2010/12/31)

A dielectric gaseous compound which exhibits the following properties: a boiling point in the range between about ?20° C. to about ?273° C.; non-ozone depleting; a GWP less than about 22,200; chemical stability, as measured by a negative standard enthalpy of formation (dHf0); a toxicity level such that when the dielectric gas leaks, the effective diluted concentration does not exceed its PEL; and a dielectric strength greater than air.

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