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6-Chloro-2-methyl-4(1H)-quinazolinone is a quinazolinone derivative with the molecular formula C10H8ClN3O. It is characterized by the presence of a chlorine atom and a methyl group attached to the quinazolinone ring. This chemical compound has been studied for its potential pharmacological properties, making it a promising candidate for various applications in the fields of pharmacology, biology, and materials science.

7142-09-8

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7142-09-8 Usage

Uses

Used in Pharmaceutical Synthesis:
6-Chloro-2-methyl-4(1H)-quinazolinone is used as a building block in the synthesis of pharmaceuticals and organic compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Antimicrobial Applications:
6-Chloro-2-methyl-4(1H)-quinazolinone has been investigated for its antimicrobial properties. It demonstrates the ability to inhibit the growth of various bacteria, making it a potential candidate for use in the development of new antimicrobial agents to combat bacterial infections.
Used in Antifungal Applications:
6-chloro-2-methyl-4(1H)-quinazolinone has also shown potential as an antifungal agent, exhibiting the ability to inhibit the growth of fungi. Its antifungal properties make it a promising candidate for use in the development of new antifungal drugs to treat fungal infections.
Used in Antiviral Applications:
6-Chloro-2-methyl-4(1H)-quinazolinone has been studied for its potential antiviral properties. It has shown the ability to inhibit the replication of certain viruses, making it a potential candidate for use in the development of new antiviral drugs to treat viral infections.
Used in Materials Science:
In addition to its biological activities, 6-chloro-2-methyl-4(1H)-quinazolinone has been utilized in the development of new materials. Its unique chemical structure and properties make it a valuable component in the creation of advanced materials with potential applications in various industries.
Used in Organic Synthesis Processes:
6-Chloro-2-methyl-4(1H)-quinazolinone has been employed in organic synthesis processes, where it serves as a key intermediate or reactant in the synthesis of various organic compounds. Its versatility and reactivity make it a valuable tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 7142-09-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7142-09:
(6*7)+(5*1)+(4*4)+(3*2)+(2*0)+(1*9)=78
78 % 10 = 8
So 7142-09-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2O/c1-5-11-8-3-2-6(10)4-7(8)9(13)12-5/h2-4H,1H3,(H,11,12,13)

7142-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-2-methylquinazolin-4(3H)-one

1.2 Other means of identification

Product number -
Other names 6-chloro-2-methyl-1H-quinazolin-4-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:7142-09-8 SDS

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