58688-30-5

Basic information

• Product Name: 2(3H)-Furanone, dihydro-3-(4-methoxybenzoyl)-
• CAS NO: 58688-30-5
• Molecular Formula: C12H12O4
• Molecular Weight: 220.225
• Mol File: 58688-30-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, dihydro-3-(4-methoxybenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, dihydro-3-(4-methoxybenzoyl)-(58688-30-5)
• EPA Substance Registry System: 2(3H)-Furanone, dihydro-3-(4-methoxybenzoyl)-(58688-30-5)

Safety Data

• Hazardous Substances Data: 58688-30-5(Hazardous Substances Data)

Upstream product

• 96-48-0 4-butanolide 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 126135-42-0 (R)-(+)-γ-(p-Methoxyphenyl)-γ-butyrolactone 
• 128994-28-5 (S)-(-)-γ-(p-Methoxyphenyl)-γ-butyrolactone 
• 27364-22-3 4-hydroxy-1-(4-methoxyphenyl)-butan-1-one 

Relevant articles and documents

A palladium-catalyzed asymmetric allylic alkylation approach to α-quaternary γ-butyrolactones

The Pd-catalyzed asymmetric allylic alkylation (Pd-AAA) of enol carbonates derived from γ-butyrolactones is reported, affording the corresponding enantioenriched α,α′-disubstituted γ-butyrolactones in both high yields and high enantioselectivities (up to 94% ee). This method was eventually applied to the synthesis of chiral spirocyclic compounds.

Unexpected reaction of a dimethylzinc-generated THF radical with aldehydes

A dimethylzinc-air-generated THF radical reacted with aldehydes at the β-position of an α-oxygenated THF.