86248-66-0

Basic information

• Product Name: 1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-5-(hydroxymeth yl)-alpha,2,5,8a-tetramethyl-, (1R-(1alpha(R*),2beta,4abeta,5beta,8aal pha))-
• Synonyms: 1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-5-(hydroxymeth yl)-alpha,2,5,8a-tetramethyl-, (1R-(1alpha(R*),2beta,4abeta,5beta,8aal pha))-;18-hydroxysclareol;(13R)-Labdan-14-ene-8,13,18-triol
• CAS NO: 86248-66-0
• Molecular Formula: C20H36O3
• Molecular Weight: 324.5
• Mol File: 86248-66-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 439.4°C at 760 mmHg
• Flash Point: 190.7°C
• Appearance: /
• Density: 1.008g/cm³
• Vapor Pressure: 1.45E-09mmHg at 25°C
• Refractive Index: 1.501
• CAS DataBase Reference: 1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-5-(hydroxymeth yl)-alpha,2,5,8a-tetramethyl-, (1R-(1alpha(R*),2beta,4abeta,5beta,8aal pha))-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-5-(hydroxymeth yl)-alpha,2,5,8a-tetramethyl-, (1R-(1alpha(R*),2beta,4abeta,5beta,8aal pha))-(86248-66-0)
• EPA Substance Registry System: 1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-5-(hydroxymeth yl)-alpha,2,5,8a-tetramethyl-, (1R-(1alpha(R*),2beta,4abeta,5beta,8aal pha))-(86248-66-0)

Safety Data

• Hazardous Substances Data: 86248-66-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C20H36O3/c1-6-18(3,22)12-8-16-19(4)11-7-10-17(2,14-21)15(19)9-13-20(16,5)23/h6,15-16,21-23H,1,7-14H2,2-5H3/t15-,16+,17+,18?,19-,20-/m0/s1

Upstream product

• 515-03-7 sclareol 

Relevant articles and documents

Microbial hydroxylation of sclareol by Rhizopus stolonifer

Incubation of sclareol with Rhizopus stolonifer affords in high yield a mixture of triols with 18-hydroxy-sclareol as the main component.

Microbial transformation of diterpenes: Hydroxylation of sclareol, manool and derivatives by Mucor plumbeus

Microbial transformation of several labd-14-ene derivatives has been carried out with a Mucor plumbeus strain. Sclareol (1) (labd-14-en-8α,13β-diol) affords quantitatively a mixture of triols from which the labd-14-en-3β,8α,13β-triol (2) is obtained in high yield. Incubation of other labdane derivatives, including manool (6) [labd-8(17),14-dien-13β-ol], the corresponding 7α-hydroxy derivative (10), manoyl oxide (14) or sclareolide (15) with the same microorganism results in a mixture of various new hydroxylated and keto-derivatives.