5720-71-8

Basic information

• Product Name: Podocarpan-14β-ol
• Synonyms: Podocarpan-14β-ol
• CAS NO: 5720-71-8
• Molecular Formula: C17H30O
• Molecular Weight: 250.4195
• Mol File: 5720-71-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Podocarpan-14β-ol(CAS DataBase Reference)
• NIST Chemistry Reference: Podocarpan-14β-ol(5720-71-8)
• EPA Substance Registry System: Podocarpan-14β-ol(5720-71-8)

Safety Data

• Hazardous Substances Data: 5720-71-8(Hazardous Substances Data)

Upstream product

• 106036-75-3 7-Keto-1-methoxy-8.8.13-trimethyl-5.6.7.8.10.13-hexahydro-phenanthren 
• 5720-80-9 8-Methoxy-1,1,4a-trimethyl-1,2,3,4,4a,9-hexahydro-phenanthren-2-ol 
• 5750-64-1 trans-1,2,3,4,9,10,11,12-Octahydro-8-hydroxy-1,1,12-trimethyl-phenanthren 
• 5720-75-2 (+/-) - 14-hydroxy-4α,4β,10α-trimethyl-3-oxo-1,2,3,4,5β,6,7,10-octahydrophenanthrene 
• 5720-78-5 (+/-) - 14-methoxy-4α,4β,10α-trimethyl-3-oxo-1,2,3,4,5β,6,7,10-octahydrophenanthrene 

Downstream Products

• 5720-73-0 8β(H)-podocarpan-14-one 

Relevant articles and documents

Total Synthesis of the Labdane Diterpenes Galanal A and B from Geraniol

The first total synthesis of galanal A and B has been achieved from naturally occurring geraniol. Key steps in this synthesis are the use of a Lewis acid assisted chiral Br?nsted acid (chiral LBA) mediated cationic polyene cyclization and a titanocene-mediated radical cyclization for the asymmetric assembly of the "AB" ring and the construction of the all-carbon quaternary center at the junction of the "BC" ring, respectively.