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2-Butenoic acid, 4,4,4-trifluoro-3-(phenylmethyl)-, ethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

198632-96-1

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198632-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198632-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,6,3 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 198632-96:
(8*1)+(7*9)+(6*8)+(5*6)+(4*3)+(3*2)+(2*9)+(1*6)=191
191 % 10 = 1
So 198632-96-1 is a valid CAS Registry Number.

198632-96-1SDS

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 3-benzyl-4,4,4-trifluorobut-2-enoate

1.2 Other means of identification

Product number -
Other names 3-benzyl-4,4,4-trifluoro-but-2-enoic acid ethyl ester

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:198632-96-1 SDS

198632-96-1Relevant academic research and scientific papers

Synthesis of β-CF3 ketones from trifluoromethylated allylic alcohols by ruthenium catalyzed isomerization

Bizet, Vincent,Pannecoucke, Xavier,Renaud, Jean-Luc,Cahard, Dominique

supporting information, p. 56 - 61 (2013/11/06)

This work describes the optimization process for the synthesis of β-trifluoromethylated ketones from trifluoromethylated allylic alcohols. This transformation proceeds through a ruthenium catalyzed isomerization under mild conditions with high atom econom

CHEMICAL COMPOUNDS

-

Page/Page column 97, (2010/02/15)

The present invention relates to novel compounds with a variety of therapeutic uses, more particularly novel naphthalene compounds that are particularly useful for selective estrogen receptor modulation.

AMINE-BASED AND AMIDE-BASED INHIBITORS OF SEMICARBAZIDE-SENSITIVE AMINE OXIDASE (SSAO) ENZYME ACTIVITY AND VAP-1 MEDIATED ADHESION USEFUL FOR TREATMENT OF DISEASES

-

Page/Page column 92, (2010/02/13)

Compositions and methods are disclosed for inhibiting semicarbazide-sensitive amine oxidase (SSAO), also known as vascular adhesion protein-1 (VAP-1). The compounds disclosed are amine-containing and amide-containing compounds. The compounds and compositions are useful for treatment of diseases, including inflammation, inflammatory diseases and autoimmune disorders.

Synthesis of 4--3-(trifluoromethyl)butanoic acid

Coe, Paul L.,Markou, Magdalini,Tatlow, John Colin

, p. 112 - 118 (2007/10/03)

Benzyl trifluoromethyl ketone and ethyl bromoacetate afforded ethyl 3-hydroxy-4-phenyl-3-(trifluoromethyl)butanoate in a Reformatsky-type reaction.This hydroxy ester, by successive stages of dehydration to a but-2-enoate, hydrogenation of the double bond,

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