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

59412-09-8

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59412-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59412-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,1 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59412-09:
(7*5)+(6*9)+(5*4)+(4*1)+(3*2)+(2*0)+(1*9)=128
128 % 10 = 8
So 59412-09-8 is a valid CAS Registry Number.

59412-09-8SDS

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 7-chloro-3-(4-methoxyphenyl)-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names 7-chloro-3-(4-methoxyphenyl)-2(1H)-quinolone

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:59412-09-8 SDS

59412-09-8Downstream Products

59412-09-8Relevant academic research and scientific papers

Quinolone derivatives

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, (2008/06/13)

A class of 2-(1H)-quinolone derivatives, substituted at the 3-position by an optionally substituted aryl substituent, are selective non-competitive antagonists of NMDA receptors and/or are antagonists of AMPA receptors, and are therefore of utility in the treatment of conditions, such as neurodegenerative disorders, convulsions or schizophrenia, which require the administration of an NMDA and/or AMPA receptor antagonist.

Carbostyril derivatives used as coccidiostats

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, (2008/06/13)

Carbostyril derivatives useful as coccidiostats are prepared by reacting an ortho-halo benzaldehyde with a 2-alkyl-2-oxazoline, then heating at above about 200° C thereby forming the carbostyril.

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