884500-73-6

Basic information

• Product Name: 2-(4-HYDROXY-PHENYL)-PYRANO[3,2-B]PYRIDIN-4-ONE
• Synonyms: 2-(4-HYDROXY-PHENYL)-PYRANO[3,2-B]PYRIDIN-4-ONE
• CAS NO: 884500-73-6
• Molecular Formula: C14H9NO3
• Molecular Weight: 0
• Mol File: 884500-73-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-HYDROXY-PHENYL)-PYRANO[3,2-B]PYRIDIN-4-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-HYDROXY-PHENYL)-PYRANO[3,2-B]PYRIDIN-4-ONE(884500-73-6)
• EPA Substance Registry System: 2-(4-HYDROXY-PHENYL)-PYRANO[3,2-B]PYRIDIN-4-ONE(884500-73-6)

Safety Data

• Hazardous Substances Data: 884500-73-6(Hazardous Substances Data)

Usage

Molecular Structure

The compound has a distinct pyrano[3,2-b]pyridin-4-one structure, which consists of a pyridine ring fused to a pyran ring.

Substituent

The presence of a hydroxy-phenyl group at the 2-position of the compound enhances its chemical properties.

Pharmacological and Therapeutic Applications

The compound has potential pharmacological and therapeutic applications due to its unique structure and functional groups.

Bioactive Properties

The compound may exhibit antioxidant, antimicrobial, or anti-inflammatory properties, making it a promising candidate for further research and development in the pharmaceutical industry.

Organic Synthesis

The compound's structure suggests it may have potential uses in organic synthesis or as a building block for the preparation of more complex molecules.

Upstream product

• 24059-83-4 3-methoxypyridine-2-carboxylic acid methyl ester 
• 62733-99-7 methyl 3-hydroxypicolinate 
• 874-24-8 3-hydroxypyridine-2-carboxylic acid 
• 884501-76-2 1-(4-methoxyphenyl)-3-(3-methoxypyridin-2-yl)propane-1,3-dione 

Relevant articles and documents

TREATMENT OF DISEASES BY EPIGENETIC REGULATION

The present disclosure provides non-naturally occurring polyphenol compounds that inhibit the bromodomain and extra terminal domain (BET) proteins. The disclosed compositions and methods can be used for treatment and prevention of cancer as well as sepsis

Synthesis of 2-aryl-4H-pyrano[2,3-b]pyridin-4-ones by a one-pot deprotection-cyclization reaction

An efficient synthesis of 2-aryl-4H-pyrano[2,3-b]pyridine-4-ones is reported, using a one-pot, two step process in the presence of pyridinium hydrochloride. The methodology is compatible with a series of functional groups useful for the synthesis of secon

PHARMACEUTICAL COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF COMPLEX DISEASES AND THEIR DELIVERY BY INSERTABLE MEDICAL DEVICES

The present invention relates to polyphenol-like compounds that are useful for inhibiting VCAM-1 expression, MCP-1 expression and/or SMC proliferation in a mammal. The disclosed compounds are useful for regulating markers of inflammatory conditions, including vascular inflammation, and for treatment and prevention of inflammatory and cardiovascular diseases and related disease states.