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125774-46-1

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125774-46-1 Usage

General Description

1,1,1-Trifluoro-3-thiophen-3-yl-propan-2-one is a chemical compound with the molecular formula C8H5F3OS. It is a synthetic organic compound which contains a trifluoromethyl group and a thiophen-3-yl group. 1,1,1-TRIFLUORO-3-THIOPHEN-3-YL-PROPAN-2-ONE is commonly used in the synthesis of a wide range of pharmaceuticals and agrochemicals. It is also used as a building block in the production of various specialty chemicals and materials. Due to its unique chemical structure, 1,1,1-trifluoro-3-thiophen-3-yl-propan-2-one exhibits specific physical and chemical properties that make it useful in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 125774-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,7 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125774-46:
(8*1)+(7*2)+(6*5)+(5*7)+(4*7)+(3*4)+(2*4)+(1*6)=141
141 % 10 = 1
So 125774-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F3OS/c8-7(9,10)6(11)3-5-1-2-12-4-5/h1-2,4H,3H2

125774-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluoro-3-thiophen-3-ylpropan-2-one

1.2 Other means of identification

Product number -
Other names S14-2863

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:125774-46-1 SDS

125774-46-1Downstream Products

125774-46-1Relevant articles and documents

-

Quinze,Laurent,Mison,Faure

, p. 211 - 232 (2007/10/02)

Secondary aziridiness, substituted by a trifluoromethyl group were prepared by reacting Grignard reagents with oximes or a N,N,N-trimethylhydrazonium salt bearing a trifluoromethyl substituent. Contrary to the results obtained with hydrogenated substrates, ethyl magnesium bromide acted exclusively as a reducing agent. The structure of aziridine 5a was determined from X-ray crystallographic data.

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