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

91366-07-3

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91366-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91366-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,6 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91366-07:
(7*9)+(6*1)+(5*3)+(4*6)+(3*6)+(2*0)+(1*7)=133
133 % 10 = 3
So 91366-07-3 is a valid CAS Registry Number.

91366-07-3SDS

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 1-methoxycarbonyl-2-methylcyclopropane-1-carboxamide

1.2 Other means of identification

Product number -
Other names (1R,2S)-1-Carbamoyl-2-methyl-cyclopropanecarboxylic acid 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:91366-07-3 SDS

91366-07-3Relevant academic research and scientific papers

Stereochemical studies on the reactions catalyzed by the PLP-dependent enzyme 1-aminocyclopropane-1-carboxylate deaminase

Liu,Auchus,Walsh

, p. 5335 - 5348 (2007/10/07)

The stereochemical course of 1-aminocyclopropane-1-carboxylate deaminase which catalyzes the fragmentation of the cyclopropane substrate to alpha -ketobutyrate and ammonia has been unraveled with the help of substrates stereospecifically labeled with deuterium and/or tritium, and this has afforded important information about the process occurring at the active site during enzymatic conversion.

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