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799783-01-0

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799783-01-0 Usage

Structure

Piperazine derivative with a methyl group and a phenyl group attached to the piperazine ring

Chirality

(3S) stereochemistry

Usage

Building block for the synthesis of biologically active compounds, ligand in metal-catalyzed reactions, and component in the production of specialty chemicals

Significance

Of interest for further investigation and study due to its potential biological and synthetic applications

Check Digit Verification of cas no

The CAS Registry Mumber 799783-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,7,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 799783-01:
(8*7)+(7*9)+(6*9)+(5*7)+(4*8)+(3*3)+(2*0)+(1*1)=250
250 % 10 = 0
So 799783-01-0 is a valid CAS Registry Number.

799783-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-methyl-1-phenylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names (S)-3-Methyl-1-phenyl-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:799783-01-0 SDS

799783-01-0Relevant articles and documents

Influence of N(2)-substitution in the alkylation of (4S)-alkyl-2,4-dihydro- 1H-pyrazino[2,1-b]quinazoline-3,6-diones

Hernandez, Fernando,Morales, Viviana,Buenadicha, Felix L.,Soellhuber, Monica,Avendano, Carmen

, p. 3045 - 3058 (2007/10/03)

1-Alkylation of O(3)-lactim, N(11)-azaenolate dilithium species derived from N(2)-H compounds 1a and 1b and the lithium azaenolates derived from the N(2)-phenyl and N(2)-(1-arylethyl) substituted compounds 2, 3 and 4 is studied. In 1 the trans-diastereose

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