20489-45-6

Basic information

• Product Name: (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol
• Synonyms: (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol;Valerianol
• CAS NO: 20489-45-6
• Molecular Formula: C₁₅H₂₆O
• Molecular Weight: 222.36634
• Mol File: 20489-45-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 309.577°C at 760 mmHg
• Flash Point: 113.14°C
• Appearance: /
• Density: 0.962g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol(20489-45-6)
• EPA Substance Registry System: (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol(20489-45-6)

Safety Data

• Hazardous Substances Data: 20489-45-6(Hazardous Substances Data)

Usage

Description

(2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol is a complex organic compound with a unique molecular structure. It is characterized by its octahydro naphthalene ring system and multiple methyl groups attached to the molecule. (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol is known for its distinct chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
(2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol can be used as a building block for the creation of more complex molecules. Its versatile structure makes it a valuable component in the synthesis of various specialty chemicals.
Used in Flavor and Fragrance Industry:
(2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol may also find applications in the flavor and fragrance industry due to its potential aromatic properties. It could be used to create unique scents or enhance the flavor profiles of various products.
Used in Research and Development:
Due to its unique structure and properties, (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol can be a valuable compound for research and development purposes. It may be used in the study of organic chemistry, molecular biology, and other related fields to explore new reactions and applications.

InChI:InChI=1/C15H26O/c1-11-6-5-7-12-8-9-13(14(2,3)16)10-15(11,12)4/h7,11,13,16H,5-6,8-10H2,1-4H3/t11-,13-,15+/m1/s1

Upstream product

• 54275-21-7 1-((2R,8R,8aS)-8,8a-dimethyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl)ethan-1-one 
• 917-54-4 methyllithium 
• 10219-75-7 valencene 

Downstream Products

• 10219-75-7 valencene 
• 20489-53-6 1,10β-Dihydro-2-oxo-11,12-anhydro-kusunol 
• 20489-54-7 (+)-tetrahydronootkatone 
• 15764-04-2 (4R,4aS)-(+)-4,4a-dimethyl-6-isopropylidene-4,4a,5,6,7,8-hexahydro-(3H)-naphthalen-2-one 
• 4674-50-4 (+)-nootkatone 
• 4630-07-3 racemic eremophilene 

Relevant articles and documents

A Stereocontrolled Entry to Racemic Eremophilane and Valencane Sesquiterpenes via an Intramolecular Diels-Alder Reaction

A stereocontrolled route to racemic eremophilane and valencane sesquiterpenes is described via a common inetrmediate 15, accessible from an intramolecular Diels-Alder rection. 13C-NMR-shift assignments of the bicyclic intermediates and products are presented.