82412-17-7

Basic information

• Product Name: (7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid
• CAS NO: 82412-17-7
• Molecular Formula: C₁₃H₁₂O₅
• Molecular Weight: 248.2314
• Mol File: 82412-17-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 471°C at 760 mmHg
• Flash Point: 184.4°C
• Density: 1.311g/cm³
• Vapor Pressure: 1.12E-09mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: (7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid(82412-17-7)
• EPA Substance Registry System: (7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid(82412-17-7)

Safety Data

• Hazardous Substances Data: 82412-17-7(Hazardous Substances Data)

Usage

General Description

(7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid is a chemical compound with the molecular formula C12H10O5. It is a derivative of 4-methylumbelliferone, a coumarin compound commonly found in plants. (7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid is a potential drug candidate for the treatment of various diseases due to its anti-inflammatory and antioxidant properties. It has also shown potential as an anti-cancer agent, particularly in the inhibition of cancer cell migration and invasion. Additionally, (7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetic acid has been investigated for its potential use in the treatment of diabetes and neurodegenerative diseases. The compound is primarily used in scientific research and has not been approved for medical use in humans.

Upstream product

• 150-19-6 O-methylresorcine 
• 108-46-3 recorcinol 
• 5852-03-9 ethyl 2-(7-hydroxy-4-methyl-2-oxo-2H-chromen-3-yl)acetate 
• 1115-30-6 diethyl acetylsuccinate 
• 95903-37-0 7-hydroxy-3-methoxycarbonylmethyl-4-methyl-2H-chromen-2-one 
• 114067-17-3 ethyl 2-(7-methoxy-4-methyl-2-oxo-2H-chromen-3-yl)acetate 
• 858753-28-3 methyl 2-(7-methoxy-4-methyl-2-oxo-2H-benzopyran-3-yl)acetate 

Relevant articles and documents

Novel photochromic 3-(3-coumarinyl)-4-(3-thienyl)maleic acid cyclic derivatives

Novel unsymmetrical photosensitive derivatives of maleic acid, anhydride and N-alkylimide, including coumarin and thiophene moieties, have been designed and synthesized; their photochromism study and fatigue resistance estimation are reported.

Modified coumarins. 25. N-acyl cytisine derivatives containing a coumarin fragment

New modified cytisine derivatives were prepared by acylation with coumarin-3-acetic acids. Springer Science+Business Media, Inc. 2007.