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2-Chloro-1,1,2-trifluoroethanethiol is a chemical compound with the molecular formula C2H2ClF3S. It is a colorless liquid at room temperature and is characterized by its strong, pungent odor. 2-chloro-1,1,2-trifluoroethanethiol is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. It is also used as a building block for the preparation of other organofluorine compounds. Due to its reactivity, it is essential to handle 2-chloro-1,1,2-trifluoroethanethiol with care, typically under controlled conditions and using appropriate safety measures.

1827-50-5

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1827-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1827-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1827-50:
(6*1)+(5*8)+(4*2)+(3*7)+(2*5)+(1*0)=85
85 % 10 = 5
So 1827-50-5 is a valid CAS Registry Number.

1827-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1,1,2-trifluoroethanethiol

1.2 Other means of identification

Product number -
Other names Ethanethiol,2-chloro-1,1,2-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:1827-50-5 SDS

1827-50-5Relevant academic research and scientific papers

Synthesis and reactivity of fluorine-containing thiols and thioacyl halides

Sizov,Kovregin,Serdyuk,Vorob'ev,Porosyatnikov,Tsvetkov,Korneev,Ermolov

, p. 1200 - 1208 (2008/02/02)

A route to α-hydropolyfluoroalkanethiols and polyfluorothioacyl halides via thermal splitting of benzyl polyfluoroalkyl sulfides under the action of phosphorus pentoxide was proposed. The thiols obtained were used as starting materials for the synthesis of α-hydropolyfluoroalkanesulfenyl chlorides. The properties of the resulting F,S-containing compounds were studied. Springer Science+Business Media, Inc. 2006.

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