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118642-72-1

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118642-72-1 Usage

General Description

2-Benzyl-4,4,4-trifluoro-3-oxobutyric acid ethyl ester is a chemical compound with the molecular formula C15H13F3O3. It is a synthetic organic compound that is commonly used in the production of pharmaceuticals and agrochemicals. 2-BENZYL-4,4,4-TRIFLUORO-3-OXOBUTYRIC ACID ETHYL ESTER is a derivative of 3-oxobutyric acid, which is an important intermediate in the synthesis of various organic compounds. 2-Benzyl-4,4,4-trifluoro-3-oxobutyric acid ethyl ester is known for its potential use as a building block in the synthesis of complex organic molecules, and it is often used in the pharmaceutical and agricultural industries for this purpose. 2-BENZYL-4,4,4-TRIFLUORO-3-OXOBUTYRIC ACID ETHYL ESTER has various applications and is sought after for its versatile chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 118642-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,4 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118642-72:
(8*1)+(7*1)+(6*8)+(5*6)+(4*4)+(3*2)+(2*7)+(1*2)=131
131 % 10 = 1
So 118642-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H13F3O3/c1-2-19-12(18)10(11(17)13(14,15)16)8-9-6-4-3-5-7-9/h3-7,10H,2,8H2,1H3

118642-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-benzyl-4,4,4-trifluoro-3-oxobutanoate

1.2 Other means of identification

Product number -
Other names Benzenepropanoic acid,a-(2,2,2-trifluoroacetyl)-,ethylester

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:118642-72-1 SDS

118642-72-1Relevant articles and documents

Studies on New Acidic Azoles as Glucose-Lowering Agents in Obese, Diabetic db/db Mice

Kees, Kenneth L.,Caggiano, Thomas J.,Steiner, Kurt E.,Fitzgerald, John J.,Kates, Michael J.,et al.

, p. 617 - 628 (1995)

Bioisosteric substitution was used as a tool to generate several new structural alternatives to the thiazolidine-2,4-dione and tetrazole heterocycles as potential antidiabetic agents.Among the initial leads that emerged from this strategy, a family of aci

Deacylative oxidation strategy for the preparation of α- functionalized carbonyls

Brodsky, Benjamin H.,Du Bois

, p. 2619 - 2621 (2007/10/03)

(Matrix Presented) α-Alkoxylation and amination of carbonyl derivatives is made possible through a unique deacylative coupling reaction that proceeds via in situ Rh-carbene formation and subsequent heteroatom-H (X-H) insertion. Reactions perform optimally

ALKYLATION DU TRIFLUOROACETYLACETATE D'ETHYLE METHODE GENERALE D'ACCES AUX TRIFLUOROMETHYLCETONES. 2eme PARTIE: ALKYLATIONS INDIRECTS DU TFAAE

Aubert, Corinne,Begue, Jean-Pierre,Charpentier-Morize, Micheline,Nee, Gerard,Langlois, Bernard

, p. 377 - 394 (2007/10/02)

A versatile method of alkylation of ethyltrifluoroacetylacetate (ETFAA) allowed selective C-alkylation of ETFAA, whatever the structure of alkyl halide was, providing that the carbonyl function was masked into a dioxolan 3 or a N,N-dimethyl hydrazone 5.These last derivatives were easily alkylated and their specific deprotection led to various C-alkylated ETFAA which in turn allowed, by a simple decarbethoxylation, the preparation of the corresponding trifluoromethyl ketones in good yields.

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