14563-35-0

Basic information

• Product Name: γ-(2,5-dimethoxyphenyl)-γ-butyrolactone
• Synonyms: γ-(2,5-dimethoxyphenyl)-γ-butyrolactone
• CAS NO: 14563-35-0
• Molecular Weight: 222.241
• Mol File: 14563-35-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: γ-(2,5-dimethoxyphenyl)-γ-butyrolactone(CAS DataBase Reference)
• NIST Chemistry Reference: γ-(2,5-dimethoxyphenyl)-γ-butyrolactone(14563-35-0)
• EPA Substance Registry System: γ-(2,5-dimethoxyphenyl)-γ-butyrolactone(14563-35-0)

Safety Data

• Hazardous Substances Data: 14563-35-0(Hazardous Substances Data)

Upstream product

• 150-78-7 1,4-dimethoxybezene 
• 1084-74-8 3-(2,5-dimethoxybenzoyl)propionic acid 

Downstream Products

• 475-38-7 5,8-Dihydroxy-1,4-naphthoquinone 

Relevant articles and documents

Catalytic Redox Chain Ring Opening of Lactones with Quinones to Synthesize Quinone-Containing Carboxylic Acids

Catalytic ring opening of five- to eight-membered lactones with quinones is achieved through a redox chain mechanism. With low loading of a simple metal triflate Lewis acid catalyst and a chain initiator, C-H bonds of many quinones were efficiently functionalized with carboxylic acid-containing side chains. This method also features 100% atom economy and wide substrate scope. A novel route to the anti-asthma drug Seratrodast was developed. Mechanism study suggests that the redox chain reaction likely undergoes a carbocation intermediate.

The reduction of beta-benzoyl-propionic acids of the resorcinol series

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