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Propanedioic acid, 2-[2-[3-(4-chlorophenyl)-3-hydroxy-1-propyn-1-yl]phenyl]-, 1,3-diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

919287-64-2

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919287-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 919287-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,2,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 919287-64:
(8*9)+(7*1)+(6*9)+(5*2)+(4*8)+(3*7)+(2*6)+(1*4)=212
212 % 10 = 2
So 919287-64-2 is a valid CAS Registry Number.

919287-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-(2-(3-(4-chlorophenyl)-3-hydroxyprop-1-ynyl)phenyl)malonate

1.2 Other means of identification

Product number -
Other names 2-{2-[3-(4-chloro-phenyl)-3-hydroxy-prop-1-ynyl]-phenyl}-malonic acid diethyl 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:919287-64-2 SDS

919287-64-2Relevant academic research and scientific papers

Highly regioselective synthesis of 2,3-disubstituted indenes via a novel palladium-catalyzed cyclization reaction of propargylic carbonates with carbon nucleophiles

Duan, Xin-Hua,Guo, Li-Na,Bi, Hai-Peng,Liu, Xue-Yuan,Liang, Yong-Min

, p. 5777 - 5780 (2007/10/03)

(Diagram presented) Palladium-catalyzed reaction of propargylic carbonates with carbon nucleophiles offers an efficient, direct route to highly substituted indenes. The reaction conditions and the scope of the process are examined, and a possible mechanis

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