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2-Butenedioic acid, 2-methyl-, 1-methyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71028-76-7

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71028-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71028-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71028-76:
(7*7)+(6*1)+(5*0)+(4*2)+(3*8)+(2*7)+(1*6)=107
107 % 10 = 7
So 71028-76-7 is a valid CAS Registry Number.

71028-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-3-methyl-4-oxobut-2-enoate

1.2 Other means of identification

Product number -
Other names 2-methyl-but-2-enedioic acid 1-methyl ester

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:71028-76-7 SDS

71028-76-7Relevant academic research and scientific papers

A three-enzyme system involving an ene-reductase for generating valuable chiral building blocks

Mangan, David,Miskelly, Iain,Moody, Thomas S.

, p. 2185 - 2190,6 (2020/09/02)

The use of ene-reductase (ERED) enzymes for the asymmetric reduction of olefins offers a green, renewable alternative to metal-catalysed asymmetric reduction. We report herein the first example of an ERED-catalysed enantiospecific reduction carried out at large scale using a carbonyl reductase (CRED) enzyme in the cofactor recycle. This reaction has been paired with a hydrolase-mediated regioselective ester hydrolysis to generate a valuable chiral building block using a straightforward one-pot process. Copyright

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