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14983-08-5

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14983-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14983-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,8 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14983-08:
(7*1)+(6*4)+(5*9)+(4*8)+(3*3)+(2*0)+(1*8)=125
125 % 10 = 5
So 14983-08-5 is a valid CAS Registry Number.

14983-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-Trifluoro-N-(3-hydroxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2,2,2-TRIFLUORO-N-(3-HYDROXYPHENYL)-ACETAMIDE

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:14983-08-5 SDS

14983-08-5Relevant articles and documents

BENZOTHIAZOLE DERIVATIVES AS ANTICANCER AGENTS

-

Page/Page column 167, (2010/06/20)

Provided is a fused heterocycle derivative showing a strong Raf inhibitory activity. A compound represented by the formula (I) wherein each symbol is as defined in the present specification, or a salt thereof.

A new, convenient and selective 4-dimethylaminopyridine-catalyzed trifluoroacetylation of anilines with ethyl trifluoroacetate

Prashad,Hu,Har,Repic,Blacklock

, p. 9957 - 9961 (2007/10/03)

A new, convenient, and selective 4-dimethylaminopyridine-catalyzed trifluoroacetylation of anilines with ethyl trifluoroacetate is described. Anilines, containing other functional groups, e.g. alcohols, phenols, hindered secondary amines, and secondary anilines, are also selectively trifluoroacetylated in high yields under these newly developed conditions. (C) 2000 Elsevier Science Ltd.

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