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5-Pyrimidinecarboxylic acid, 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-phenyl-1-(phenylmethyl)-, methyl ester, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

865086-56-2

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865086-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 865086-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,0,8 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 865086-56:
(8*8)+(7*6)+(6*5)+(5*0)+(4*8)+(3*6)+(2*5)+(1*6)=202
202 % 10 = 2
So 865086-56-2 is a valid CAS Registry Number.

865086-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydro-6-methyl-2-oxo-4-phenyl-1-(phenylmethyl)-(4S)-5-pyrimidinecarboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names (S)-1-benzyl-6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic methyl ester

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:865086-56-2 SDS

865086-56-2Downstream Products

865086-56-2Relevant academic research and scientific papers

CHIRAL AMINE-CATALYZED ASYMMETRIC ADDITION OF CARBON-CENTERED NUCLEOPHILES TO IMINES

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Page/Page column 36-37; 70, (2010/11/25)

The present invention relates to an asymmetric synthesis useful for preparing compounds useful for the treatment of cardiovascular diseases and for studying the role of motor proteins in cell cycle progression.

Asymmetric Mannich reactions of β-keto esters with acyl imines catalyzed by cinchona alkaloids

Lou, Sha,Taoka, Brandon M.,Ting, Amal,Schaus, Scott E.

, p. 11256 - 11257 (2007/10/03)

Cinchona alkaloids catalyze the enantioselective Mannich reaction of β-keto esters with acyl aryl imines. The reaction requires 10 mol % of cinchonine or cinchonidine. The reaction products are obtained in good yields (81-99%), high enantioselectivities (

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