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4,7-dichloro-2-benzofuran-1(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52043-46-6

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52043-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52043-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,4 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52043-46:
(7*5)+(6*2)+(5*0)+(4*4)+(3*3)+(2*4)+(1*6)=86
86 % 10 = 6
So 52043-46-6 is a valid CAS Registry Number.

52043-46-6SDS

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 4,7-dichloro-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names 4,7-Dichlorophthalide

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:52043-46-6 SDS

52043-46-6Downstream Products

52043-46-6Relevant academic research and scientific papers

Synthesis and SAR of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones related to licostinel (Acea 1021) as NMDA/glycine site antagonists

Zhou, Zhang-Lin,Kher, Sunil M.,Cai, Sui Xiong,Whittemore, Edward R.,Espitia, Stephen A.,Hawkinson, Jon E.,Tran, Minhtam,Woodward, Richard M.,Weber, Eckard,Keana, John F. W.

, p. 1769 - 1780 (2007/10/03)

A series of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones (QXs) related to licostinel (Acea 1021) was synthesized and evaluated as antagonists for the glycine site of the N-methyl-D-asparate (NMDA) receptor. The in vitro potency of these

Synthesis of phosphonate 3-phthalidyl esters as prodrugs for potential intracellular delivery of phosphonates

Dang, Qun,Brown, Brian S.,Van Poelje, Paul D.,Colby, Timothy J.,Erion, Mark D.

, p. 1505 - 1510 (2007/10/03)

A new prodrug approach for intracellular delivery of phosphonates was developed via the synthesis of 3-phthalidyl esters of 1- naphthalenemethylphosphonate. This approach is advantageous over the traditional acyloxymethyl phosphonate prodrugs, because the

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