127-36-6

Basic information

• Product Name: 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol
• Synonyms: Einecs 204-836-9;1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol;1,2,3,4,4a,4b,5,6,7,9,10,10a-Dodecahydro-1,4a-dimethyl-7-isopropyl-1-phenanthrenemethanol;(1R-(1alpha,4Abeta,4balpha,10aalpha))-dodecahydro-1,4A-dimethyl-7-(1-methylethyl)-1-phenanthrenemethanol;1-Phenanthrenemethanol, 1,2,3,4,4A,4B,5,6,7,9,10,10A-dodecahydro-1,4A-dimethyl-7-(1-methylethyl)-
• CAS NO: 127-36-6
• Molecular Formula: C20H34O
• Molecular Weight: 290.48336
• EINECS: 204-836-9
• Mol File: 127-36-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol(127-36-6)
• EPA Substance Registry System: 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-7-isopropyl-1,4a-dimethylphenanthren-1-methanol(127-36-6)

Safety Data

• Hazardous Substances Data: 127-36-6(Hazardous Substances Data)

Usage

Class

Polycyclic aromatic hydrocarbons

Backbone

Dodecahydro-7-isopropyl-1,4a-dimethylphenanthrene

Functional group

Hydroxyl group

Attachment

First carbon atom

Potential applications

Pharmaceuticals

Biological activities

Possible due to the presence of the hydroxyl group

Further research

Required to fully understand properties and potential uses

Complexity

Highly complex organic compound

Number of carbon atoms

21 (dodecahydro indicates 12 hydrogen atoms attached to the carbon backbone)

Isopropyl group

Attached to the 7th carbon atom

Dimethyl groups

Attached to the 1st and 4a carbon atoms

Hydrogenation

Fully saturated (dodecahydro indicates complete hydrogenation)

Chirality

4a position may exhibit chirality (presence of a stereocenter)

Solubility

Likely to be more soluble in organic solvents due to its hydrophobic nature

Stability

Relatively stable due to the presence of multiple aromatic rings

Melting point

Not provided, but expected to be relatively high for a fully saturated compound

Boiling point

Not provided, but expected to be relatively high due to its large molecular size and complexity

Density

Not provided, but expected to be higher than water due to its nonpolar nature

Optical activity

May exhibit optical activity if the 4a position is chiral

Reactivity

Potential for reactions at the hydroxyl group, such as esterification, etherification, or oxidation

InChI:InChI=1/C20H34O/c1-14(2)15-6-8-17-16(12-15)7-9-18-19(3,13-21)10-5-11-20(17,18)4/h12,14-15,17-18,21H,5-11,13H2,1-4H3