76508-32-2

Basic information

• Product Name: (3aR,4R,6aR)-4-Octyl-2,6-dioxo-hexahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester
• Synonyms: (3aR,4R,6aR)-4-Octyl-2,6-dioxo-hexahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester
• CAS NO: 76508-32-2
• Molecular Weight: 418.487
• Mol File: 76508-32-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3aR,4R,6aR)-4-Octyl-2,6-dioxo-hexahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3aR,4R,6aR)-4-Octyl-2,6-dioxo-hexahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester(76508-32-2)
• EPA Substance Registry System: (3aR,4R,6aR)-4-Octyl-2,6-dioxo-hexahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester(76508-32-2)

Safety Data

• Hazardous Substances Data: 76508-32-2(Hazardous Substances Data)

Upstream product

• 76311-91-6 3-Bromo-5-octyl-5H-furan-2-one 
• 17756-68-2 5-octyl-5H-furan-2-one 
• 76508-30-0 (3aR,4R,6aR)-2-Amino-4-octyl-6-oxo-3a,4,6,6a-tetrahydro-furo[3,4-b]furan-3-carboxylic acid 4-methoxy-benzyl ester 

Downstream Products

• 26057-70-5 (+/-)-avenaciolide 

Relevant articles and documents

TOTAL SYNTHESIS OF (+/-)-AVENACIOLIDE AND ITS ANALOGUES

A new method for the stereoselective synthesis of (+/-)-avenaciolide and its analogues via methoxycarbonyl- or anisyloxycarbonyldi-γ-lactones, which could be easily prepared by the reaction of γ-substituted α-bromobutenolides with sodium salt of methyl or anisyl malonamate in good yields, was described.