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(E)-But-2-enedioic acid (1S,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76529-73-2

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76529-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76529-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76529-73:
(7*7)+(6*6)+(5*5)+(4*2)+(3*9)+(2*7)+(1*3)=162
162 % 10 = 2
So 76529-73-2 is a valid CAS Registry Number.

76529-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-menthyl methyl fumarate

1.2 Other means of identification

Product number -
Other names methyl-((1R)-menthyl)-fumarate

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:76529-73-2 SDS

76529-73-2Relevant academic research and scientific papers

Diastereoselectivities in the Diels-Alder reactions of cyclopentadiene with optically active dimenthyl fumarate and menthyl methyl fumarate in LiClO4/ether and on Al2O3

Bains,Pagni,Kabalka,Pala

, p. 821 - 834 (2007/10/02)

Reactions of cyclopentadiene with (-)-dimenthyl fumarate, which yield adducts 1 and 2, and with (-)-menthyl methyl fumarate, which yield adducts 3 through 6, were carried out on alumina activated at different temperatures, in LiClO4/ether solut

A Simple, Powerful, and Efficient Method for Transesterification

Meth-Cohn, Otto

, p. 695 - 697 (2007/10/02)

Aromatic and α,β-unsaturated methyl esters undergo efficient transesterification at ambient temperature or below with primary, secondary, or (particularly) tertiary alcohols in the presence of butyl-lithium in tetrahydrofuran solution.

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