111189-35-6

Basic information

• Product Name: 2-(phenanthren-9-yl)cyclohexanol
• Synonyms: 2-(9-Phenanthrenyl)cyclohexanol; Cyclohexanol, 2-(9-phenanthrenyl)-
• CAS NO: 111189-35-6
• Molecular Formula: C₂₀H₂₀O
• Molecular Weight: 276.3722
• Mol File: 111189-35-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 485.9°C at 760 mmHg
• Flash Point: 186.2°C
• Density: 1.171g/cm³
• Vapor Pressure: 2.95E-10mmHg at 25°C
• Refractive Index: 1.682
• CAS DataBase Reference: 2-(phenanthren-9-yl)cyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(phenanthren-9-yl)cyclohexanol(111189-35-6)
• EPA Substance Registry System: 2-(phenanthren-9-yl)cyclohexanol(111189-35-6)

Safety Data

• Hazardous Substances Data: 111189-35-6(Hazardous Substances Data)

Usage

Chemical composition

Consists of a cyclohexane ring attached to a phenanthrene group.

Physical form

White to off-white solid.

Solubility

Sparingly soluble in water.

Usage

Primarily used in research and development activities as a precursor to synthesize other organic compounds.

Application in pharmaceutical industry

Used as an intermediate for manufacturing various drugs.

Potential applications

Has potential applications in the field of materials science and organic synthesis.

Safety precautions

Proper safety precautions should be followed when handling and using this compound.

Upstream product

• 573-17-1 9-bromophenanthrene 
• 286-20-4 cyclohexane-1,2-epoxide 
• 73129-94-9 2-(phenanthren-9-yl)cyclohexanone 

Downstream Products

• 205-99-2 benzo[e]acephenanthrylene 
• 73129-94-9 2-(phenanthren-9-yl)cyclohexanone 

Relevant articles and documents

Palladium-catalyzed asymmetric hydrogenation of 2-aryl cyclic ketones for the synthesis oftranscycloalkanols through dynamic kinetic resolution under acidic conditions

The first efficient palladium-catalyzed asymmetric hydrogenation of 2-aryl cyclic ketones has been described through dynamic kinetic resolution under acidic conditions, providing a facile access to chiraltranscycloalkanol derivatives with excellent enantioselectivities.

Trans-2-Arylcyclohexanols: Use as auxiliaries in the mukaiyama aldol-type condensation between silyl enol esters and aldehydes

trans-2-Aryclohexanols 2a, 2b proved to be efficient auxiliaries esters in the Mukaiyama aldol-type condensation of silyl enol esters 4 with aldehydes.