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286838-85-5

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286838-85-5 Usage

Structure

2,5-Piperazinedione derivative with a methyl and 2-methylpropylidene substituent attached to the nitrogen atoms

Configuration

6Z, indicating a particular arrangement of double bonds in the molecule

Usage

in the pharmaceutical and chemical industries as a building block for organic synthesis and as a precursor for the production of pharmaceutical compounds

Potential

pharmacological activities, making it a potential candidate for drug development

Additional research needed

to fully understand its potential applications and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 286838-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,6,8,3 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 286838-85:
(8*2)+(7*8)+(6*6)+(5*8)+(4*3)+(3*8)+(2*8)+(1*5)=205
205 % 10 = 5
So 286838-85-5 is a valid CAS Registry Number.

286838-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-6-(2-methylpropylidene)piperazine-2,5-dione

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:286838-85-5 SDS

286838-85-5Downstream Products

286838-85-5Relevant articles and documents

Unusual C=C bond migration in 3-ylidene-2,5-piperazinediones

Jin, Shangde,Wessig, Pablo,Liebscher, Ju?rgen

, p. 1993 - 1999 (2007/10/03)

Treatment of 3-alkylidene or 3-benzylidene-2,5-piperazinediones 6 with catalytic amounts of acid gives rise to the formation of isomers 7 by migration of the C=C bond into the alkyl substituent at position 6, or results in mixtures of racemic 7 and E isomers 8. The existence of tautomeric equilibria is discussed.

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