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Propanoic acid, 3-[(methoxycarbonyl)amino]-2-methyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

270075-30-4

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270075-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 270075-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,0,7 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 270075-30:
(8*2)+(7*7)+(6*0)+(5*0)+(4*7)+(3*5)+(2*3)+(1*0)=114
114 % 10 = 4
So 270075-30-4 is a valid CAS Registry Number.

270075-30-4SDS

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 methyl 3-((methoxycarbonyl)amino)-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names methyl ((methoxycarbonyl)amino)-2-methyl propanoate

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:270075-30-4 SDS

270075-30-4Downstream Products

270075-30-4Relevant academic research and scientific papers

Hofmann-type rearrangement of imides by in situ generation of imide-hypervalent iodines(III) from iodoarenes

Moriyama, Katsuhiko,Ishida, Kazuma,Togo, Hideo

supporting information; experimental part, p. 946 - 949 (2012/05/05)

The Hofmann-type rearrangement of aromatic and aliphatic imides using a hypervalent iodine(III) reagent generated in situ from PhI, m-CPBA, and TsOH·H2O proceeded in the presence of a base in alcohol to provide anthranilic acid derivatives and amino acid derivatives in high yields, respectively. This reaction proceeds through a tandem reaction via alcoholysis followed by a Hofmann rearrangement promoted by the formation of an imide-λ3-iodane intermediate.

Effect of catalytic alkali metal bromide on Hofmann-type rearrangement of imides

Moriyama, Katsuhiko,Ishida, Kazuma,Togo, Hideo

supporting information; experimental part, p. 8574 - 8576 (2012/09/07)

The Hofmann-type rearrangement of aromatic and aliphatic imides using KBr as the catalyst proceeded to provide aromatic and aliphatic amino acid derivatives. We have also developed a new synthetic route to gabapentin with this method.

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