184376-10-1

Basic information

• Product Name: 5-hydroxy-4-(4-methoxy-phenyl)-5H-furan-2-one
• Synonyms: 5-hydroxy-4-(4-methoxy-phenyl)-5H-furan-2-one
• CAS NO: 184376-10-1
• Molecular Weight: 206.198
• Mol File: 184376-10-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-hydroxy-4-(4-methoxy-phenyl)-5H-furan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-hydroxy-4-(4-methoxy-phenyl)-5H-furan-2-one(184376-10-1)
• EPA Substance Registry System: 5-hydroxy-4-(4-methoxy-phenyl)-5H-furan-2-one(184376-10-1)

Safety Data

• Hazardous Substances Data: 184376-10-1(Hazardous Substances Data)

Upstream product

• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 5703-26-4 4-Methoxyphenylacetaldehyde 
• 563-96-2 2,2-dihydroxyacetic acid 
• 914362-13-3 4-(4-methoxy-phenyl)-5-(tetrahydro-pyran-2-yloxy)-5H-furan-2-one 
• 298-12-4 Glyoxilic acid 
• 5720-07-0 4-methoxyphenylboronic acid 
• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 

Downstream Products

• 1005402-35-6 5-(4-methoxyphenyl)-2-methyl-2H-pyridazin-3-one 
• 1364247-79-9 5-[4-(3-chloropropoxy)phenyl]-2-(3-methylpyridin-2-yl)-2H-pyridazin-3-one 
• 1364245-50-0 5-[4-(3-chloropropoxy)phenyl]-2-(6-methylpyridin-2-yl)-2H-pyridazin-3-one 
• 1005402-38-9 5-[4-(3-chloropropoxy)phenyl]-2-methyl-2H-pyridazin-3-one 
• 1353387-77-5 5-(4-hydroxyphenyl)-2-(3-methylpyridin-2-yl)-2H-pyridazin-3-one 
• 1005402-44-7 5-(4-hydroxyphenyl)-2-(6-methylpyridin-2-yl)-2H-pyridazin-3-one 
• 1005402-37-8 5-(4-hydroxyphenyl)-2-methyl-2H-pyridazin-3-one 
• 1364234-78-5 5-(4-methoxyphenyl)-2-(3-methylpyridin-2-yl)-2H-pyridazin-3-one 
• 1005402-43-6 5-(4-methoxyphenyl)-2-(6-methylpyridin-2-yl)-2H-pyridazin-3-one 
• 32136-81-5 alpha-methoxy-4-hydroxyacetophenone 
• 123564-56-7 (±)-hydroxybutenolide 

Relevant articles and documents

Access to Bromo-γ-butenolides via Zwitterion-Catalyzed Rearrangement of Cyclopropene Carboxylic Acids

γ-Butenolides are useful structural motifs in many pharmaceutically relevant compounds. In particular, halogenated γ-butenolides are attractive building blocks because the halogen handles can readily be manipulated to give various functional molecules. In

Pyridizinone derivatives

The present invention provides compounds of formula (I*): their use as H3 inhibitors, processes for their preparation, and pharmaceutical compositions thereof.

Syntheses of bryophyte constituents. 8. Sphagnum acid and its degradation products

For Sphagnum acid (1) and its enzymatic degradation product 5-hydroxy-4-(4-hydroxyphenyl)-5H-furan-2-on (2) efficient syntheses on preparative scale were developed. For the (4-hydroxyphenyl)butenolide 2 some characteristic chemical transformations are observed in acidic and basic medium. Johann Ambrosius Barth 1996.