70955-71-4
3-[5,5,6-TRIMETHYLBICYCLO[2.2.1]HEPT-2-YL]CYCLOHEXAN-1-OL
CAS: 70955-71-4
Molecular Formula: C16H28O
70955-71-4 - Names and Identifiers
70955-71-4 - Physico-chemical Properties
| Molecular Formula | C16H28O |
| Molar Mass | 236.39 |
| Density | 0.97g/mLat 25°C(lit.) |
| Boling Point | 302°C(lit.) |
| Flash Point | >230°F |
| Refractive Index | n20/D 1.496(lit.) |
70955-71-4 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/38 - Irritating to eyes and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 2 |
70955-71-4 - Introduction
The product of the reaction of 2-methoxyphenol with hydro-2, 2-dimethyl-3-methylenebicyclo [2.2.1] heptane is 2-methoxy-5, 6-dihydro-2, 2,5,6-Tetramethylbicyclo [2.2.1] heptan-1-one. The product has the following properties and uses:
Nature:
-Appearance: colorless liquid
-Molecular formula: C12H22O
-Molecular weight: 182.31g/mol
-Boiling point: About 180 ° C
-Density: about 0.84 g/mL
-Melting point: approx. -10 ° C
Use:
-2-methoxy-5, 6-dihydro-2, 2,5, 6-Tetramethylbicyclo [2.2.1] heptan-1-one is an important organic synthesis intermediate, which can be used to synthesize drugs, fragrances and dyes.
-It can also be used as a hydrogenating agent and reducing agent in organic synthesis reactions, and has certain application value in the field of chemical research.
Preparation Method:
The reaction of 2-methoxy phenol with hydrogenated -2,2-dimethyl -3-methylene bicyclo [2.2.1] heptane is generally carried out in an organic solvent (such as toluene, dichloromethane, etc.), commonly used catalysts such as platinum chloride and platinum sulfate. The reaction conditions are generally room temperature or heated reaction.
Safety Information:
-2-methoxy-5, 6-dihydro-2, 2,5, 6-Tetramethylbicyclo [2.2.1] heptan-1-one is irritating and corrosive to the skin and eyes. After contact, rinse with plenty of water immediately and seek help from a doctor.
-During use or storage, attention should be paid to avoid contact with oxidants, acids, alkalis and other substances, and avoid high temperatures and open flames.
-Wear appropriate protective equipment such as gloves, goggles, and lab clothes when performing related experiments or operations.
-When handling this compound, follow proper laboratory practices and properly dispose of waste. In case of any doubt or accident, seek professional help immediately.
Nature:
-Appearance: colorless liquid
-Molecular formula: C12H22O
-Molecular weight: 182.31g/mol
-Boiling point: About 180 ° C
-Density: about 0.84 g/mL
-Melting point: approx. -10 ° C
Use:
-2-methoxy-5, 6-dihydro-2, 2,5, 6-Tetramethylbicyclo [2.2.1] heptan-1-one is an important organic synthesis intermediate, which can be used to synthesize drugs, fragrances and dyes.
-It can also be used as a hydrogenating agent and reducing agent in organic synthesis reactions, and has certain application value in the field of chemical research.
Preparation Method:
The reaction of 2-methoxy phenol with hydrogenated -2,2-dimethyl -3-methylene bicyclo [2.2.1] heptane is generally carried out in an organic solvent (such as toluene, dichloromethane, etc.), commonly used catalysts such as platinum chloride and platinum sulfate. The reaction conditions are generally room temperature or heated reaction.
Safety Information:
-2-methoxy-5, 6-dihydro-2, 2,5, 6-Tetramethylbicyclo [2.2.1] heptan-1-one is irritating and corrosive to the skin and eyes. After contact, rinse with plenty of water immediately and seek help from a doctor.
-During use or storage, attention should be paid to avoid contact with oxidants, acids, alkalis and other substances, and avoid high temperatures and open flames.
-Wear appropriate protective equipment such as gloves, goggles, and lab clothes when performing related experiments or operations.
-When handling this compound, follow proper laboratory practices and properly dispose of waste. In case of any doubt or accident, seek professional help immediately.
Last Update：2024-04-09 15:16:30
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