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(2E)-3-[3-(trifluoromethyl)phenyl]prop-2-enamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93040-58-5

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93040-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93040-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93040-58:
(7*9)+(6*3)+(5*0)+(4*4)+(3*0)+(2*5)+(1*8)=115
115 % 10 = 5
So 93040-58-5 is a valid CAS Registry Number.

93040-58-5SDS

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 3-(3-(trifluoromethyl)phenyl)-2-Propenamide

1.2 Other means of identification

Product number -
Other names -

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:93040-58-5 SDS

93040-58-5Relevant academic research and scientific papers

Novel oxazoles, their manufacture and use as pharmaceutical agents

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Page/Page column 7, (2008/06/13)

The present invention relates to novel oxazoles of formula (I) their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, medicaments containing them and their manufacture

Synthesis, structure and quantitative structure-activity relationships of σ receptor ligands, 1-[2-(3,4-dimethoxyphenyl)ethyl]-4-(3-phenylpropyl)piperazines

Fujimura, Ken-Ichi,Matsumoto, Junzo,Niwa, Masashi,Kobayashi, Tadayuki,Kawashima, Yoichi,In, Yasuko,Ishida, Toshimasa

, p. 1675 - 1683 (2007/10/03)

A set of the title compounds having different substituents (R1, R2) on their phenyl groups was synthesized to find σ receptor binding affinity. Among the compounds, 2b (R1=R2=Cl) has the most potent σ1-binding activity, while 2a (R1=R2=H, SA4503) was most selective to σ1 over σ2 receptor. The crystal structures of 2a and 2b were shown, by X-ray crystallography, to be similar except for the one torsional angle of their propylene parts. Quantitative structure-activity relationship study suggested the affinity of the compounds to the σ1 receptor was dependent on the electronic feature, Swain-Lupton's R or S(π) that was derived by molecular orbital method, of R1 and R2.

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