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alpha,alpha,4-trimethylphenethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71617-15-7

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71617-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71617-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,1 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71617-15:
(7*7)+(6*1)+(5*6)+(4*1)+(3*7)+(2*1)+(1*5)=117
117 % 10 = 7
So 71617-15-7 is a valid CAS Registry Number.

71617-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-methyl-1-(4-methylphenyl)propan-2-yl] acetate

1.2 Other means of identification

Product number -
Other names 2-methyl-1-(4-methylphenyl)propan-2-yl acetate

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:71617-15-7 SDS

71617-15-7Downstream Products

71617-15-7Relevant academic research and scientific papers

Hypervalent iodine(III)-mediated decarboxylative acetoxylation at tertiary and benzylic carbon centers

Kiyokawa, Kensuke,Okumatsu, Daichi,Minakata, Satoshi

supporting information, p. 1046 - 1050 (2019/11/11)

The decarboxylative acetoxylation of carboxylic acids using a combination of PhI(OAc)2 and I2 in a CH2Cl2/AcOH mixed solvent is reported. The reaction was successfully applied to two types of carboxylic acids containing an α-quaternary and a benzylic carbon center under mild reaction conditions. The resulting acetates were readily converted into the corresponding alcohols by hydrolysis.

TEMPERATURE DEPENDENCE OF ACTIVATION VOLUME FOR ACETOLYSIS OF 2-ARYL-2-METHYLPROPYL TOSYLATES

Sera, Akira,Yamada, Hiroaki,Masaki, Hitoshi

, p. 1533 - 1536 (2007/10/02)

The activation volume of the acetolysis of the title compounds was found to have an unexpectedly large temperature dependence.The activation volume-temperature profile of a steep concave was observed which was responsible for the previously reported anomaly of the substituent dependence of the activation volume.

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