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162965-54-0

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162965-54-0 Usage

General Description

2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE is a chemical compound with the formula C7H6F3NS. It is a pyridine derivative containing a trifluoroethylthio functional group. 2-[(2,2,2-TRIFLUOROETHYL)THIO]-PYRIDINE is used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It has also been studied for its potential biological and pharmacological activities. Additionally, it is known for its use as a building block in organic synthesis and as a reagent in chemical reactions. However, it is important to handle this chemical with care as it may have potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 162965-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,6 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 162965-54:
(8*1)+(7*6)+(6*2)+(5*9)+(4*6)+(3*5)+(2*5)+(1*4)=160
160 % 10 = 0
So 162965-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NS/c8-7(9,10)5-12-6-3-1-2-4-11-6/h1-4H,5H2

162965-54-0SDS

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 2-(2,2,2-trifluoroethylsulfanyl)pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2-[(2,2,2-trifluoroethyl)thio]

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:162965-54-0 SDS

162965-54-0Downstream Products

162965-54-0Relevant articles and documents

Synthesis of aryl 2,2,2-trifluoroethyl sulfides

Menczinger, Bálint,Nemes, Anikó,Szabó, Dénes,Schlosser, Gitta,Jernei, Tamás,Csámpai, Antal,Rábai, József

, (2020/01/28)

Aryl 2,2,2-trifluoroethyl sulfides were synthesized by copper(I)-catalyzed nucleophilic aromatic substitution reaction (Goldberg-Ullmann coupling). The method requires aryl iodides and 2,2,2-trifluoroethyl thioacetate as starting materials, benzylamine as solvent and base, and copper(I) bromide as a catalyst. The reaction mixture was stirred at 110 °C for 6 h under inert atmosphere to afford the targeted aryl 2,2,2-trifluoroethyl sulfides in moderate to good yield.

Process for preparing trifluoroethyl sulfur compounds from thiolates and 1-chloro-2,2,2-trifluoroethane

-

, (2008/06/13)

Process for preparing trifluoroethyl sulfur compounds from thiolates and 1-chloro-2,2,2-trifluoroethane. The invention relates to the preparation of trifluoroethyl sulfur compounds of the formula RSCH2 CF3 by reacting 1-chloro-2,2,2-

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