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131747-57-4

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131747-57-4 Usage

General Description

"(2-Trifluoromethyl-pyridin-3-yl)-methanol" is a specialized chemical compound that includes elements of pyridine, methanol, and trifluoromethyl groups. The pyridine segment represents a basic six-membered ring compound, consisting of one nitrogen atom, and five carbon atoms, often used in synthesizing various drugs. The methanol group, a form of alcohol, features one carbon atom bonded to three hydrogen atoms and one hydroxyl group. Lastly, the trifluoromethyl aspect includes a carbon atom attached to three fluorine atoms, known for its role in enhancing the biological activity of many drugs. The nature and arrangement of these components indicate that this compound may be typically utilized in chemical research, potentially in the pharmaceutical field, although specific applications may vary.

Check Digit Verification of cas no

The CAS Registry Mumber 131747-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131747-57:
(8*1)+(7*3)+(6*1)+(5*7)+(4*4)+(3*7)+(2*5)+(1*7)=124
124 % 10 = 4
So 131747-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6F3NO/c8-7(9,10)6-5(4-12)2-1-3-11-6/h1-3,12H,4H2

131747-57-4SDS

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 [2-(trifluoromethyl)pyridin-3-yl]methanol

1.2 Other means of identification

Product number -
Other names (2-(trifluoromethyl)pyridin-3-yl)methanol

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:131747-57-4 SDS

131747-57-4Relevant articles and documents

Modular Route to Azaindanes

Huang, Qi,Zard, Samir Z.

, p. 3895 - 3898 (2017/07/26)

A convergent radical based route to azaindanes is described, relying on the degenerative addition transfer of various substituted S-(pyridylmethyl)-O-ethyl dithiocarbonates (xanthates) to functional alkenes followed by radical cyclization onto the pyridine ring activated by protonation with trifluoroacetic acid. In one case, a richly decorated cyclohepta[b]pyridine could be assembled swiftly by allowing the first adduct to N-phenylmaleimide to undergo addition to N-allylphthalimide prior to cyclization.

Heterocyclic chalcone activators of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) with improved in vivo efficacy

Lounsbury, Nicole,Mateo, George,Jones, Brielle,Papaiahgari, Srinivas,Thimmulappa, Rajash K.,Teijaro, Christiana,Gordon, John,Korzekwa, Kenneth,Ye, Min,Allaway, Graham,Abou-Gharbia, Magid,Biswal, Shyam,Childers, Wayne

supporting information, p. 5352 - 5359 (2015/11/11)

Nrf2 activators represent a good drug target for designing agents to treat diseases associated with oxidative stress. Building upon previous work, we designed and prepared a series of heterocyclic chalcone-based Nrf2 activators with reduced lipophilicity

COMPOSITIONS AND METHODS FOR MODULATING FXR

-

Page/Page column 123, (2012/07/13)

The present invention relates to compounds of Formula (I), a stereoisomer, enantiomer, a pharmaceutically acceptable salt or an amino acid conjugate thereof; wherein variables are as defined herein; and their pharmaceutical compositions, which are useful as modulators of the activity of Farnesiod X receptors (FXR).

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