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2,4(1H,3H)-Pyrimidinedione, dihydro-5-methyl-1-[(1R)-1-phenylethyl]-, (5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

252579-98-9

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252579-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252579-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,5,7 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 252579-98:
(8*2)+(7*5)+(6*2)+(5*5)+(4*7)+(3*9)+(2*9)+(1*8)=169
169 % 10 = 9
So 252579-98-9 is a valid CAS Registry Number.

252579-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1'R,5S)-1-(1'-phenylethyl)-5-methyldihydropyrimidin-2,4-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:252579-98-9 SDS

252579-98-9Upstream product

252579-98-9Downstream Products

252579-98-9Relevant academic research and scientific papers

Enantioselective synthesis of α,β-substituted β-amino acids

Agami, Claude,Cheramy, Sandrine,Dechoux, Luc,Melaimi, Mohand

, p. 195 - 200 (2007/10/03)

Chiral derivative 3 was shown to be a precursor of α and β-substituted β-amino acids as well as α,β-disubstituted β-amino acids. The key steps of the procedure are a diastereoselective alkylation of synthon 3 by organocuprates reagents and a diastereoselective alkylation of the alkylated adduct.

Stereoselective α-alkylation of new chiral auxiliaries: An access to enantiomerically pure α- and α,β-substituted β-amino acids

Agami, Claude,Cheramy, Sandrine,Dechoux, Luc

, p. 1838 - 1840 (2007/10/03)

New bicyclic heterocycles 5, which are potentially useful for the enantioselective synthesis of substituted β-amino acids, have been synthesized. A study on the α-alkylation of these chiral auxiliaries is presented. An optically pure β-amino acid was obtained in excellent yield from its masked chiral derivative 6a.

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