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2,5-Piperazinedione, 3,6-bis(chlorophenylmethyl)-3,6-dimethoxy-1,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87264-22-0

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87264-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87264-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,6 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87264-22:
(7*8)+(6*7)+(5*2)+(4*6)+(3*4)+(2*2)+(1*2)=150
150 % 10 = 0
So 87264-22-0 is a valid CAS Registry Number.

87264-22-0SDS

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 3,6-di(α-chlorobenzyl)-3,6-dimethoxy-1,4-dimethylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3,6-Bis-(chloro-phenyl-methyl)-3,6-dimethoxy-1,4-dimethyl-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:87264-22-0 SDS

87264-22-0Relevant academic research and scientific papers

Pyrazine Chemistry. V. Synthesis of Methylanhydropicroroccellin and Dimethylpicroroccellin

Marcuccio, Sebastian M.,Elix, John A.

, p. 1785 - 1796 (2007/10/02)

The structure of the lichen diketopiperazine, picroroccellin, has been studied by the synthesis of several of its degradation products.The three possible formulations of methylanhydropicroroccellin (3), (4) and (5) were synthesized and from the physical and chemical properties, the former two compounds were shown to be dissimilar from the naturally derived material.Furthermore, the reactivity of the 3-methoxypiperazine-2,5-dione (5) entirely paralleled that reported for picroroccellin and was consistent with the oxygen functions being located at the 3- and 6-positionsof the piperazine-2,5-dione ring.Dimethylpicroroccellin (23) was synthesized, so establishing the trans-stereochemistry of this compound.The properties of (23) were identical with those recorded for the naturally derived material.Hence we conclude that picroroccellin should be reformulated as (2).

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