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Benzenemethanol, 3,4,5-trifluoro-a-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923033-01-6

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923033-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923033-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,3 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 923033-01:
(8*9)+(7*2)+(6*3)+(5*0)+(4*3)+(3*3)+(2*0)+(1*1)=126
126 % 10 = 6
So 923033-01-6 is a valid CAS Registry Number.

923033-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4,5-trifluorophenyl)ethanol

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:923033-01-6 SDS

923033-01-6Relevant academic research and scientific papers

Umpolung of protons from H2O: A metal-free chemoselective reduction of carbonyl compounds: Via B2pin2/H2O systems

Xuan, Qingqing,Zhao, Cong,Song, Qiuling

supporting information, p. 5140 - 5144 (2017/07/11)

H2O is routinely described as a proton donor, however, in the presence of diboron compounds, the umpolung reaction of H2O under metal-free conditions was successfully developed, which could afford hydride species, leading to a highly efficient and chemoselective reduction of CO bonds. This strategy exhibits excellent chemoselectivities toward carbonyl groups in the presence of ester, olefin, halogen, thioether, sulfonyl, cyano as well as heteroaromatic groups.

N-(ARYLAMINO)-SULFONAMIDE INHIBITORS OF MEK

-

Page/Page column 94; 95, (2008/06/13)

This invention concerns N-(2-arylamino) aryl sulfonamides, which are inhibitors of MEK and are useful in treatment of cancer and other hyperproliferative diseases.

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