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4-Acetylphenol trifluoroacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31083-17-7

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31083-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31083-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31083-17:
(7*3)+(6*1)+(5*0)+(4*8)+(3*3)+(2*1)+(1*7)=77
77 % 10 = 7
So 31083-17-7 is a valid CAS Registry Number.

31083-17-7SDS

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 4-acetylphenyl triflate

1.2 Other means of identification

Product number -
Other names p-Acetylphenyltrifluoracetat

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:31083-17-7 SDS

31083-17-7Relevant academic research and scientific papers

Acid-Catalyzed Thermal Decomposition of 1-Aryl-3,3-dialkyltriazenes in the Presence of Nucleophiles

Satyamurthy, N.,Barrio, Jorge R.,Schmidt, Derrick G.,Kammerer, Craig,Bida, Gerald T.,Phelps, Michael E.

, p. 4560 - 4564 (2007/10/02)

The acid-catalyzed thermal decompositions of a number of 1-aryl-3,3-dialkyltriazenes (1) in the presence of nucleophiles have been conducted with a view to understanding the underlying mechanisms of these reactions.These reactions parallel the corresponding diazonium ion reactions in that a heterolytic dediazoniation path competes with a homolytic route.The relative proportion of the products arising due to these two competing mechanisms depends upon (a) the electron-transfer efficiency of the nucleophile, (b) the redox potential of the aryl diazonium substrate, and (c) the reaction solvent.

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