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4-(o-Chlorobenzylidene)-2-methyloxazol-5(4H)-one is an oxazol-5(4H)-one derivative, a class of heterocyclic organic compounds characterized by the presence of a chlorobenzylidene group and a methyl group on the oxazol ring. This complex chemical compound possesses a range of biological activities, such as anti-inflammatory and antimicrobial properties, making it a promising candidate for pharmaceutical applications and other research areas.

32997-15-2

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32997-15-2 Usage

Uses

Used in Pharmaceutical Industry:
4-(o-Chlorobenzylidene)-2-methyloxazol-5(4H)-one is used as a pharmaceutical compound for its demonstrated anti-inflammatory properties, which can be harnessed to develop treatments for various inflammatory conditions. Its antimicrobial activity also suggests potential applications in the development of new antibiotics or antimicrobial agents to combat resistant strains of bacteria.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-(o-Chlorobenzylidene)-2-methyloxazol-5(4H)-one serves as a valuable target for synthesis and study. Researchers can explore its chemical and physical properties to understand its mechanisms of action and optimize its therapeutic potential, potentially leading to the discovery of novel drugs with improved efficacy and safety profiles.
Used in Drug Synthesis:
4-(o-Chlorobenzylidene)-2-methyloxazol-5(4H)-one's unique structure and biological activities make it a candidate for drug synthesis, where it can be further modified or combined with other molecules to create new pharmaceutical agents with specific therapeutic targets and improved pharmacological properties.
Used in Laboratory Studies:
4-(o-Chlorobenzylidene)-2-methyloxazol-5(4H)-one is utilized in laboratory settings for the investigation of its biological activities and potential applications. Researchers can study its interactions with biological systems, such as cell lines or animal models, to gain insights into its therapeutic potential and mechanisms of action, ultimately contributing to the advancement of medical knowledge and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 32997-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32997-15:
(7*3)+(6*2)+(5*9)+(4*9)+(3*7)+(2*1)+(1*5)=142
142 % 10 = 2
So 32997-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H8ClNO2/c1-7-13-10(11(14)15-7)6-8-4-2-3-5-9(8)12/h2-6H,1H3/b10-6-

32997-15-2SDS

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 4-[(2-chlorophenyl)methylidene]-2-methyl-1,3-oxazol-5-one

1.2 Other means of identification

Product number -
Other names 4-o-Chlorbenzyliden-2-methyloxazol-5-on

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:32997-15-2 SDS

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