1452899-95-4

Basic information

• Product Name: (3S)-3-(4-tert-butylphenyl)-5-methyl-3-(prop-2-en-1-yl)-2,3-dihydrofuran-2-one
• CAS NO: 1452899-95-4
• Molecular Weight: 270.371
• Mol File: 1452899-95-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S)-3-(4-tert-butylphenyl)-5-methyl-3-(prop-2-en-1-yl)-2,3-dihydrofuran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3S)-3-(4-tert-butylphenyl)-5-methyl-3-(prop-2-en-1-yl)-2,3-dihydrofuran-2-one(1452899-95-4)
• EPA Substance Registry System: (3S)-3-(4-tert-butylphenyl)-5-methyl-3-(prop-2-en-1-yl)-2,3-dihydrofuran-2-one(1452899-95-4)

Safety Data

• Hazardous Substances Data: 1452899-95-4(Hazardous Substances Data)

Upstream product

• 1452899-76-1 3-(4-tert-butylphenyl)-5-methyl-2,5-dihydrofuran-2-one 
• 76311-90-5 5-methyl-3-bromo-2(5H)-furanone 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 1452899-79-4 3-(4-tert-butylphenyl)-5-methylfuran-2-yl prop-2-en-1-yl carbonate 

Relevant articles and documents

Palladium-catalyzed asymmetric allylic alkylation of cyclic dienol carbonates: Efficient route to enantioenriched γ-butenolides bearing an all-carbon α-quaternary stereogenic center

Alpha, beta, gamma: Allyl dienol carbonates (1) served as substrates for the title reaction to afford the furanones 2 in both high yields and high enantioselectivities. These furanones were eventually converted into valuable building blocks including γ-tertiary and γ-quaternary furanones (3) as well as β-quaternary butyrolactones (4). This method was used as a key step in the total synthesis of (-)-nephrosteranic acid and (-)-roccellaric acid. Copyright