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Phosphonic acid, [5-chloro-2-(phenylethynyl)phenyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

639516-95-3

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639516-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 639516-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,9,5,1 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 639516-95:
(8*6)+(7*3)+(6*9)+(5*5)+(4*1)+(3*6)+(2*9)+(1*5)=193
193 % 10 = 3
So 639516-95-3 is a valid CAS Registry Number.

639516-95-3SDS

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 (5-chloro-2-phenylethynyl-phenyl)-phosphonic acid diethyl ester

1.2 Other means of identification

Product number -
Other names (5-chloro-2-phenylethynylphenyl)phosphonic 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:639516-95-3 SDS

639516-95-3Relevant academic research and scientific papers

Phosphaisocoumarins as a new class of potent inhibitors for pancreatic cholesterol esterase

Li, Baojian,Zhou, Binhua,Lu, Hailiang,Ma, Lin,Peng, Ai-Yun

experimental part, p. 1955 - 1963 (2010/06/20)

Due to the importance of pancreatic cholesterol esterase (CEase) as a potential target in atherosclerosis and for the development of hypocholesterolemic agents, there are increasing interests in designing and synthesizing CEase inhibitors. In the present study, we prepared forty-five isocoumarin phosphorus analogues (i.e., phosphaisocoumarins) and investigated the inhibition of these compounds on the CEase. The results showed that some phosphaisocoumarins could act as potent inhibitors of CEase. The most potent inhibitors, compounds 9d, 10a and 12e give IC50 values of 4.8?μM, 2.3?μM and 1.9?μM, respectively. The inhibition mechanism and kinetic characterization studies indicate that they are reversible competitive inhibitors.

A convenient and applicable route to synthesize 2-(1-alkynyl) phenylphosphonates

Peng, Ai-Yun,Zhang, Xin-Ying,Ding, Yi-Xiang

, p. 529 - 534 (2007/10/03)

A convenient and applicable route has been developed to synthesize various 2-(1-alkynyl)-phenylphosphonates starting from easily available phenols via palladium-catalyzed alkynyl dehydroxylation of 2-hydroxylphenylphosphonates.

Synthesis of phosphaisocoumarins via iodocyclization

Peng, Ai-Yun,Ding, Yi-Xiang

, p. 1119 - 1121 (2007/10/03)

4-Iodophosphaisocoumarins can be prepared in good yield and with high regioselectivity under mild conditions by the reaction of o-(1-alkynyl) phenylphosphonates with I2 or ICI. The present reaction represents the first example of a phosphonate

The Synthesis of Phosphaisocoumarins by Cu(I)-Catalyzed Intramolecular Cyclization of o-Ethynylphenylphosphonic Acid Monoesters

Peng, Ai-Yun,Ding, Yi-Xiang

, p. 15006 - 15007 (2007/10/03)

Cu(I)-catalyzed intramolecular cyclization of o-ethynylphenylphosphonic acid monoethyl esters was examined, and a new class of six-membered phosphorus heterocycles was formed with high regioselectivity and good yields. The present reaction is the first ex

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