2-(7,7-Dimethylbicyclo[2.2.1]-2-heptyl)-cyclohexanol
2(3 or 4)-(7,7-dimethylbicyclo[2.2.1]hept-2-yl)cyclohexan-1-ol
CAS: 69834-10-2
Molecular Formula: C15H26O
2-(7,7-Dimethylbicyclo[2.2.1]-2-heptyl)-cyclohexanol - Names and Identifiers
2-(7,7-Dimethylbicyclo[2.2.1]-2-heptyl)-cyclohexanol - Physico-chemical Properties
| Molecular Formula | C15H26O |
| Molar Mass | 222.37 |
2-(7,7-Dimethylbicyclo[2.2.1]-2-heptyl)-cyclohexanol - Introduction
2(3 or 4)-(7,7-Dimethylbicyclo [2.2.1] hept-2-yl) cyclohexan-1-ol is an organic compound. The following is a description of its properties, uses, preparation methods and safety information:
Nature:
2(3 or 4)-(7,7-Dimethylbicyclo [2.2.1] hept-2-yl) cyclohexan-1-ol is a colorless to slightly yellow liquid. It is volatile at room temperature and soluble in many organic solvents.
Use:
This compound is often used as an intermediate in chemical synthesis. It can be used to build C- C bonds in organic synthesis reactions, for example, it plays an important role in the Chernikov reaction.
Preparation Method:
The synthesis of 2(3 or 4)-(7,7-dimethylbicyclo [2.2.1] hept-2-yl) cyclohexan-1-ol is usually accomplished by a chemical reaction. A common preparation method is by reaction of cyclohexanone with lithium (7,7-dimethylbicyclo [2.2.1] hept-2-yl) aluminum or lithium aluminum hydride, followed by reduction to give the target compound.
Safety Information:
Nature:
2(3 or 4)-(7,7-Dimethylbicyclo [2.2.1] hept-2-yl) cyclohexan-1-ol is a colorless to slightly yellow liquid. It is volatile at room temperature and soluble in many organic solvents.
Use:
This compound is often used as an intermediate in chemical synthesis. It can be used to build C- C bonds in organic synthesis reactions, for example, it plays an important role in the Chernikov reaction.
Preparation Method:
The synthesis of 2(3 or 4)-(7,7-dimethylbicyclo [2.2.1] hept-2-yl) cyclohexan-1-ol is usually accomplished by a chemical reaction. A common preparation method is by reaction of cyclohexanone with lithium (7,7-dimethylbicyclo [2.2.1] hept-2-yl) aluminum or lithium aluminum hydride, followed by reduction to give the target compound.
Safety Information:
Last Update：2024-04-09 01:59:57
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