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2-Aziridinecarboxylicacid,1-(2-cyanoethyl)-,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86649-90-3

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86649-90-3 Usage

Chemical class

Aziridinecarboxylic acids

Uses

Intermediate in pharmaceutical and agricultural industries, building block in organic and medicinal chemistry research

Physical properties

Colorless or pale yellow liquid, characteristic odor

Health hazards

Moderate toxicity, potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 86649-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,4 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86649-90:
(7*8)+(6*6)+(5*6)+(4*4)+(3*9)+(2*9)+(1*0)=183
183 % 10 = 3
So 86649-90-3 is a valid CAS Registry Number.

86649-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-cyanoethyl)aziridine-2-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

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:86649-90-3 SDS

86649-90-3Downstream Products

86649-90-3Relevant academic research and scientific papers

REACTIONS OF AZIRIDINE-2-CARBOXYLIC ACID DERIVATIVES WITH ESTERS AND NITRILES OF UNSATURATED ACIDS

Trapentsier, P. T.,Kalvin'sh, I. Ya.,Liepin'sh, E'. E'.,Lukevits, E'. Ya.

, p. 391 - 394 (1983)

Products of addition to the multiple bond were obtained in the reaction of the methyl ester, nitrile, and amide of aziridine-2-carboxylic acid with esters or nitriles of acrylic acid and esters of maleic, acetylenemonocarboxylic, and acetylenedicarboxylic acids.The bromination of 1-(2-alkoxycarbonylethenyl)-2-methoxycarbonylaziridines under various conditions leads to the addition of bromine to the multiple bond with retention or opening of the aziridine ring.

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