10207-79-1

Basic information

• Product Name: (+)-Isoabeinol
• Synonyms: (+)-Isoabeinol;(1R,4aα)-Decahydro-2,5,5,8aβ-tetramethyl-1-(3-methylene-4-pentenyl)naphthalen-2α-ol;Isoabienol;Labda-13(16),14-diene-8-ol;Labdane F2
• CAS NO: 10207-79-1
• Molecular Formula: C₂₀H₃₄O
• Molecular Weight: 290.48336
• Mol File: 10207-79-1.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (+)-Isoabeinol(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-Isoabeinol(10207-79-1)
• EPA Substance Registry System: (+)-Isoabeinol(10207-79-1)

Safety Data

• Hazardous Substances Data: 10207-79-1(Hazardous Substances Data)

Usage

General Description

(+)-Isoabeinol is a naturally occurring chemical compound that is classified as a diterpene. It is found in the bark and wood of several tree species, including the Japanese and Chinese red pine. (+)-Isoabeinol has been isolated and studied for its potential medicinal properties, including anti-inflammatory and analgesic effects. Research has also suggested that (+)-Isoabeinol may have antimicrobial and anti-tumor properties, making it a potentially valuable compound for pharmaceutical and biotechnological applications. However, further studies are needed to fully understand the pharmacological and biological activities of this compound.

Upstream product

• 22628-64-4 Acetic acid (1R,2R,4aS,8aS)-2,5,5,8a-tetramethyl-1-(3-methylene-pent-4-enyl)-decahydro-naphthalen-2-yl ester 
• 22628-57-5 Acetic acid (1R,2R,4aS,8aS)-2,5,5,8a-tetramethyl-1-((E)-3-methyl-penta-2,4-dienyl)-decahydro-naphthalen-2-yl ester 
• 22628-62-2 8α-acetoxy-13R-hydroxy-labda-14-ene 
• 54274-72-5 (R)-5-((1R,2R,4aS,8aS)-2-acetoxy-2,5,5,8a-tetramethyldecahydronaphthalen-1-yl)-3-methylpent-1-en-3-yl acetate 
• 515-03-7 sclareol 

Downstream Products

• 468-84-8 ambreinolide 

Relevant articles and documents

Oxidative degradation of the sclareol side chain: hemisyntheses of ambergris derivatives using in the key steps palladium complexes or ruthenium tetroxide generated in situ

We report the hemisyntheses of various ambergris-type derivatives: ambraoxide 4, Ambrox 8, 13-methylambraoxide 13, ambraketal 14, norambraketal 15, non-norambraketal 16 and dioxepane 53.Sclareol 12 is used as starting material because it is currently available from Salvia sclarea.The key steps involve an oxidative degradation of the sclareol 12 side chain, using either palladium complexes or ruthenium tetroxide generated in situ. - Keywords: sclareol; Ambrox; ambraoxide; 13-methylambraoxide; ambraketal; norambraketal; nor-norambraketal; farnesylic aldehyde; palladium complex; ruthenium tetroxide generated in situ; oxidative degradation