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Acetamide, 2,2,2-trifluoro-N-(3-hydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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 academic research and scientific papers

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.

Mild debenzylation of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene as a non-lewis-basic cation scavenger

Okano, Kentaro,Okuyama, Kei-Ichiro,Fukuyama, Tohru,Tokuyama, Hidetoshi

experimental part, p. 1977 - 1980 (2009/04/07)

Scope and limitations of the debenzylation conditions for aryl benzyl ether, which was developed during our synthetic studies on yatakemycin, were investigated. The chemoselective debenzylation proceeds at low temperature with a combination of BCl3 and pentamethylbenzene as a cation scavenger in the presence of various functional groups.

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.

Phosphorus in organic synthesis. Acyloxyphosphonium salts as chemoselective acylating reagents

Froyen, Paul

, p. 5359 - 5362 (2007/10/03)

Acyloxytriphenylphosphonium salts 1 prepared in situ react with a variety of aminophenols to give the corresponding amides in excellent yields. At -25°N-acylated products are formed exclusively, whereas 0°some O-acylated products are observed. 1 is also a

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