59056-72-3 - Names and Identifiers
Name | 1-(octahydro-7,7,8,8-tetramethyl-2,3b-methano-3bH-cyclopenta[1,3]cyclopropa[1,2]benzen-4-yl)ethanone
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Synonyms | Einecs 261-584-2 1-(octahydro-7,7,8,8-tetramethyl-2,3b-methano-3bH-cyclopenta[1,3]cyclopropa[1,2]benzen-4-yl)ethanone Ethanone, 1-(octahydro-7,7,8,8-tetramethyl-2,3B-methano-3bh-cyclopenta(1,3)cyclopropa(1,2)benzen-4-yl)-
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CAS | 59056-72-3
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EINECS | 261-584-2 |
59056-72-3 - Physico-chemical Properties
Molecular Formula | C17H26O
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Molar Mass | 246.38774 |
59056-72-3 - Introduction
1-(octahydro-7,7,8,8-tetramethyl-2, benzen-4-yl)ethanone is an organic compound, it is also known as OCB(Octahydrocyclopenta[1,3] cyclopapa [1,2]benzene).
Nature:
OCB is a solid with a colorless to pale yellow appearance. It has a low vapor pressure at room temperature and low solubility. Its molecular formula is C16H24O, and it has a cyclic structure and a carbonyl functional group in the chemical structure.
Use:
OCB is widely used in chemical research and industrial manufacturing, as an intermediate for the synthesis of other organic compounds. It is used as an ingredient in flavors and fragrances to give products a unique smell. In addition, OCB can also be used for the synthesis of hetero-chelate ligands, the preparation of organic photocatalysts and other organic synthesis starting materials.
Preparation Method:
The preparation method of OCB is more complicated, and a common synthesis method is to synthesize by chemical reaction. Specific methods include cyclization reactions, alkylation, carbonylation reactions, and the like.
Safety Information:
Information on the safety and toxicity of OCB is limited. Therefore, caution should be exercised when using OCB. Good laboratory safety practices should be followed, including wearing appropriate protective equipment (e. G. Gloves, goggles) and ensuring that the operation is carried out in well-ventilated conditions. In case of ingestion or exposure, seek medical attention immediately and provide details of the compound.
Last Update:2024-04-10 22:29:15