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3,6-Methylene-2,5-piperazinedione is an organic compound that is identified as an impurity in Cycloserine, which is an antibacterial agent. It is characterized by its molecular structure that includes a methylene bridge between the 3 and 6 positions of the piperazinedione core.

15996-22-2

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15996-22-2 Usage

Uses

Used in Pharmaceutical Industry:
3,6-Methylene-2,5-piperazinedione is used as an impurity in the production of Cycloserine (C988800), an antibacterial agent. Its presence is significant as it can impact the quality, safety, and efficacy of the final drug product. The pharmaceutical industry must monitor and control the levels of this impurity to ensure the therapeutic effectiveness and safety profile of Cycloserine.

Check Digit Verification of cas no

The CAS Registry Mumber 15996-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15996-22:
(7*1)+(6*5)+(5*9)+(4*9)+(3*6)+(2*2)+(1*2)=142
142 % 10 = 2
So 15996-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-3-5(9)8-4(2)6(10)7-3/h1-2H2,(H,7,10)(H,8,9)

15996-22-2SDS

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 3,6-dimethylidenepiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3,6-dimethylene-piperazine-2,5-dione

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:15996-22-2 SDS

15996-22-2Downstream Products

15996-22-2Relevant academic research and scientific papers

An efficient and facile synthesis of D-cycloserine substantially free from potential impurities

Awasthi, Arun Kumar,Kumar, Brijesh,Aga, Mushtaq A,Tripathi, Punit,Reddy, Cirandur Suresh,Kumar, Pramod

, p. 1248 - 1253 (2017)

An efficient and facile synthesis of D-cycloserine has been developed from D-serine with 61% overall yield employing protectiondeprotection strategy. Different parameters affecting the impurities content and yield of D-cycloserine have been studied. Mild reaction conditions provided the product with remarkable purity (>99%) and high stability.

Concise approach to the syntheses of (±)-gliocladin C and related diketopiperazine alkaloids

Hodges, Timothy R.,Benjamin, Noah M.,Martin, Stephen F.

, p. 3329 - 3338 (2018)

A unique approach to the diketopiperazine indole alkaloid (±)-gliocladin C was developed and applied to formal syntheses of the related alkaloids (±)-gliocladine C and (±)-T988C. The key features of the strategy include an unprecedented nucleophilic addition of a diketopiperazine to an isatin derivative followed by a Friedel-Crafts alkylation of the resultant tertiary alcohol with indole to establish the critical quaternary center. Subsequent reduction of the intermediate oxindole moiety and cyclization then delivered a pivotal hexahydropyrrolo[2,3-b]indole diketopiperazine intermediate that was readily converted into (±)-gliocladin C as well as racemic versions of key intermediates in the Overman syntheses of (+)-gliocladine C and (+)-T988C.

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