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630423-35-7

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630423-35-7 Usage

General Description

The chemical compound 7-chloro-4-methoxy-1(2H)-quinolinone is a heterocyclic compound with a quinolinone core structure that contains chlorine and methoxy groups attached to the quinoline ring. It is also known as Clioquinol and is a halogenated 8-hydroxyquinoline derivative. 7-Chloro-4-Methoxy-1(2H)-... has antibacterial and antifungal properties and has been used in topical medications for the treatment of various skin infections. It has also been studied for its potential neuroprotective and anticancer properties. 7-chloro-4-methoxy-1(2H)-quinolinone is a versatile chemical with diverse applications in medicine and research.

Check Digit Verification of cas no

The CAS Registry Mumber 630423-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,0,4,2 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 630423-35:
(8*6)+(7*3)+(6*0)+(5*4)+(4*2)+(3*3)+(2*3)+(1*5)=117
117 % 10 = 7
So 630423-35-7 is a valid CAS Registry Number.

630423-35-7SDS

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 7-Chloro-4-methoxy-1(2H)-isoquinolinone

1.2 Other means of identification

Product number -
Other names 7-chloro-4-methoxy-2H-isoquinolin-1-one

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:630423-35-7 SDS

630423-35-7Relevant articles and documents

Process for Synthesizing Substituted Isoquinolines

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Page/Page column 11-12, (2010/04/23)

The present disclosure generally relates to a process for synthesizing optionally substituted 1-chloro-4-methoxyisoquinolines. The present disclosure also relates to intermediates useful in this process.

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