483-66-9

Basic information

• Product Name: sphondin
• Synonyms: sphondin;6-Methoxy-2H-furo[2,3-h][1]benzopyran-2-one;6-Methoxy-2H-furo[2,3-h]-1-benzopyran-2-one;2H-Furo(2,3-h)-1-benzopyran-2-one, 6-Methoxy-
• CAS NO: 483-66-9
• Molecular Formula: C₁₂H₈O₄
• Molecular Weight: 216.19312
• Mol File: 483-66-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 189-191 °C
• Boiling Point: 413 °C at 760 mmHg
• Flash Point: 203.6 °C
• Appearance: /
• Density: 1.368 g/cm³
• Vapor Pressure: 4.96E-07mmHg at 25°C
• Refractive Index: 1.635
• Storage Temp.: 2-8°C
• CAS DataBase Reference: sphondin(CAS DataBase Reference)
• NIST Chemistry Reference: sphondin(483-66-9)
• EPA Substance Registry System: sphondin(483-66-9)

Safety Data

• Hazardous Substances Data: 483-66-9(Hazardous Substances Data)

Usage

General Description

Sphondin is a chemical compound found in certain plants and is classified as a coumarin derivative. It is known for its anticoagulant and antithrombotic properties, making it potentially beneficial for preventing blood clot formation. Sphondin has also been studied for its potential as an anti-inflammatory and anti-cancer agent, with research indicating that it may have inhibitory effects on certain cancer cells. Additionally, sphondin has been found to exhibit antioxidant activity, which can help protect cells from oxidative stress and damage. Overall, sphondin is a compound with diverse potential health benefits and is the subject of ongoing research for its medicinal properties.

InChI:InChI=1/C12H8O4/c1-14-9-6-7-2-3-10(13)16-11(7)8-4-5-15-12(8)9/h2-6H,1H3

Upstream product

• 61265-07-4 heratomol 
• 77-78-1 dimethyl sulfate 
• 116663-86-6 3-Benzenesulfinyl-6-methoxy-3,4-dihydro-2H-furo[2,3-h]chromene 
• 116663-85-5 6-methoxy-3-(phenylthio)-(2,3,4H)-furo<2,3-h><1>benzopyran 
• 250639-95-3 6-benzyloxy-furo[2,3-h]chromen-2-one 
• 462094-30-0 2-[(6-methoxy-2-oxo-2H-chromen-7-yl)oxy]acetaldehyde 
• 116669-19-3 6-methoxy-2-oxo-3-(phenylthio)-(2,3,4H)-furo<2,3-h><1>benzopyran 
• 116663-87-7 6-methoxy-(2H)-furo<2,3-h>-1-benzopyran 

Downstream Products

• 574-84-5 7,8-dihydroxy-6-methoxy-2H-1-benzopyran-2-one 

Relevant articles and documents

Ring-closing-metathesis-based synthesis of annellated coumarins from 8-allylcoumarins

8-Allylcoumarins are conveniently accessible through a microwave-promoted tandem Claisen rearrangement/Wittig olefination/ cyclization sequence. They serve as a versatile platform for the annellation of five- to seven-membered rings using ring-closing ole

Synthesis and antifungal activity of coumarins and angular furanocoumarins

Angelicin, a naturally occurring furanocoumarin, that showed antifungal activity, was considered as a lead structure for a group of synthetic coumarins. Antifungal activities of the synthesized coumarins and angelicin derivatives were reported against Can