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Aziridine-2,3-dione, also known as ethylenedinitrile or 2,3-dihydro-1H-azirine-2,3(3aH)-dione, is a heterocyclic compound with the molecular formula C2H2N2O2. It features a three-membered ring structure with two carbon atoms and one nitrogen atom, and two carbonyl groups (C=O) attached to the carbon atoms. aziridine-2,3-dione is highly reactive due to the strained three-membered ring and the presence of electron-withdrawing nitrile groups, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Aziridine-2,3-dione is also known for its potential as a chemical warfare agent due to its toxicity and ability to inhibit acetylcholinesterase, an enzyme crucial for the proper functioning of the nervous system.

598-60-7

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598-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 598-60-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 598-60:
(5*5)+(4*9)+(3*8)+(2*6)+(1*0)=97
97 % 10 = 7
So 598-60-7 is a valid CAS Registry Number.
InChI:InChI=1/C2HNO2/c4-1-2(5)3-1/h(H,3,4,5)

598-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name aziridine-2,3-dione

1.2 Other means of identification

Product number -
Other names Oximide

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:598-60-7 SDS

598-60-7Downstream Products

598-60-7Relevant academic research and scientific papers

Process for the preparation of penem compounds and intermediates for this preparation

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, (2008/06/13)

Compounds of the general formula I in which, X denotes a halogen atom;, Y denotes a hydrogen atom, a halogen atom, or a moiety of the general formula II Z denotes a halogen atom, a hydroxy group, a substituted hydroxy group, an -S(O)nR5 group, or an -Se(O)mR5 group;, n denotes 0, 1 or 2, preferably 0 or 1;, m denotes 0 or 1;, R3 denotes a hydrogen atom or an organic group;, R4 denotes a hydrogen atom, a carboxy-salt-forming ion, or a carboxy-ester-forming group;, R5 denotes a hydrogen atom, a hydrocarbon group, or a heterocyclyl group; and, R12 denotes a hydrogen atom, an unsubstituted or substituted hydrocarbon group, or an unsubstituted or substituted heterocyclyl group;, are novel intermediates useful in the preparation of 6-methylene-penems of the general formula X:

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