170711-93-0

Basic information

• Product Name: 6α-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one
• CAS NO: 170711-93-0
• Molecular Weight: 316.441
• Mol File: 170711-93-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6α-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6α-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one(170711-93-0)
• EPA Substance Registry System: 6α-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one(170711-93-0)

Safety Data

• Hazardous Substances Data: 170711-93-0(Hazardous Substances Data)

Upstream product

• 18676-07-8 (-)-Hispanolone 
• 82462-69-9 6β-acetoxy-15,16-epoxylabda-8,13(16),14-trien-7-one 
• 151-50-8 potassium cyanide 
• 82462-67-7 (+)-(4aS,8aS)-4-[2-(3-furyl)ethyl]-4a,5,6,7,8,8a-hexahydro-3,4a,8,8-tetramethylnaphthalen-2(1H)-one 
• 866003-58-9 15,16-epoxy-8(9),13(16),14-labdatrien-6β,7β-diol 

Relevant articles and documents

The absolute stereochemistry of a diterpene from Ballota aucheri

The semi-synthetic transformation of hispanolone, isolated from Ballota africana, into βp-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one has established an ent-labdane absolute stereochemistry for a diterpene metabolite originally isolated from B. aucheri.

Synthesis of sibiricinone A, sibiricinone B and leoheterin

Two labdenolides, sibiricinone A and sibericinone B, and a furo-labdane leoheterin have been synthesized from sclareol, for the first time, establishing in this manner the absolute configuration for these compounds.