112953-47-6

Basic information

• Product Name: {[5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxy}acetic acid
• CAS NO: 112953-47-6
• Molecular Formula: C₁₈H₁₃ClO₅
• Molecular Weight: 344.7458
• Mol File: 112953-47-6.mol

Chemical Properties

• Boiling Point: 568.3°C at 760 mmHg
• Flash Point: 297.5°C
• Density: 1.42g/cm³
• Vapor Pressure: 9.44E-14mmHg at 25°C
• Refractive Index: 1.634
• CAS DataBase Reference: {[5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxy}acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: {[5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxy}acetic acid(112953-47-6)
• EPA Substance Registry System: {[5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxy}acetic acid(112953-47-6)

Safety Data

• Hazardous Substances Data: 112953-47-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Applications:
[5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxyacetic acid is used as a potential drug candidate for [application reason] its possible anti-inflammatory or antioxidant properties, which could be beneficial in the treatment of various medical conditions.
Used in Fluorescent Dye Applications:
In the field of chemical research and analysis, [5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxyacetic acid is used as a potential fluorescent dye for [application reason] its chromone backbone, which may offer unique fluorescence properties useful in various analytical techniques.
Used in Treatment of Oxidative Stress-Related Diseases:
[5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxyacetic acid is used as a potential therapeutic agent for [application reason] its suggested potential in treating diseases associated with oxidative stress, due to its chromone structure and possible antioxidant properties.
Used in Chemical Research:
In the chemical research industry, [5-chloro-3-(2-methylphenyl)-4-oxo-4H-chromen-7-yl]oxyacetic acid is used as a synthetic compound for [application reason] further investigation into its properties, potential applications, and the development of new drugs or materials based on its unique structure.

Upstream product

• 112953-73-8 Ethyl <(5-chloro-3-(2-methylphenyl)-4-oxo-4H-1-benzopyran-7-yl)oxy>acetate 
• 7051-16-3 1-chloro-3,5-dimethoxybenzene 
• 112953-92-1 5-Chloro-7-hydroxy-3-(2-methylphenyl)-4-oxo-4H-1-benzopyran 
• 112954-18-4 1-(2-chloro-6-hydroxy-4-methoxy)phenyl-2-(2-methylphenyl)-1-ethanone 
• 112954-14-0 5-Chloro-7-methoxy-3-(2-methylphenyl)-4-oxo-4H-1-benzopyran 
• 10166-09-3 (o-tolyl)acetyl chloride 

Relevant articles and documents

Aryloxyacetic acid diuretics with uricosuric activity. II. Substituted [(4-oxo-4H-1-benzopyran-7-yl)oxy]acetic acids and the related compounds

Di- and tri-substituted [(4-oxo-4H-1-benzopyran-7-yl)oxy]acetic acids, and 4-oxo-3-phenyl-4H-furo[2,3-h][1]benzopyran-8-carboxylic acid were synthesized and tested for natriuretic and uricosuric activities. Among the compounds tested, 3,5-disubstituted [(4-oxo-4H-1-benzopyran-7-yl)oxy]acetic acids (6c-f, h, n and x) showed potent natriuretic and uricosuric activities, whereas 4-oxo-3-phenyl-4H-furo[2,3-h][1]benzopyran-8-carboxylic acid (6dd) possessed only potent natriuretic activity. The structure-activity relationships are also discussed.

Benzopyran derivatives

A benzopyran derivative represented by formula STR1 wherein: R1 and R2 each represents a hydrogen atom, a lower alkyl group, a substituted or unsubstituted cyclic alkyl group, a mono- or di-lower alkylamino group, a substituted or un