trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer
CAS: 29855-05-8
Molecular Formula: C15H24O
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer - Names and Identifiers
| Name | trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer |
| Synonyms | trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer |
| CAS | 29855-05-8 |
| EINECS | 249-893-0 |
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer - Physico-chemical Properties
| Molecular Formula | C15H24O |
| Molar Mass | 220.35046 |
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene, stereoisomer - Introduction
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene is an oxygen-containing natural organic compound, which is a stereoisomer. Its chemical formula is C15H22O, and its molecular structure has a 13-member macrocycle and a continuous double bond, in which the four methyl groups of the molecule are connected to the macrocycle.
Regarding its properties, trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene is a colorless liquid with a peculiar aromatic odor. It is unstable at room temperature and is prone to polymerization or self-condensation reactions.
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene is widely used. It can be used as a starting material for organic synthesis and for the synthesis of other organic compounds, such as lubricants, fragrances, fungicides, etc. It can also be used as an organic electrochromic material or a photosensitive material for optical and electronic devices.
The method of preparing trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene includes a specific organic synthesis route. The common method is to synthesize its skeleton structure through step synthesis or tandem reaction, appropriate functional modifications are then made.
Regarding safety information, as trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene has high reactivity at room temperature, so care should be taken when handling. It is irritating to the eyes, skin and respiratory tract and should be used with appropriate protective measures such as laboratory gloves, goggles and protective face masks. At the same time, avoid inhaling its vapor or dust, and keep away from ignition sources and oxidants. In the use or storage, should follow the appropriate safety procedures, and properly dispose of waste. It is best to use the compound under professional guidance.
Regarding its properties, trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene is a colorless liquid with a peculiar aromatic odor. It is unstable at room temperature and is prone to polymerization or self-condensation reactions.
trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene is widely used. It can be used as a starting material for organic synthesis and for the synthesis of other organic compounds, such as lubricants, fragrances, fungicides, etc. It can also be used as an organic electrochromic material or a photosensitive material for optical and electronic devices.
The method of preparing trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene includes a specific organic synthesis route. The common method is to synthesize its skeleton structure through step synthesis or tandem reaction, appropriate functional modifications are then made.
Regarding safety information, as trimethyl-13-oxabicyclo[10.1.0]trideca-4,8-diene has high reactivity at room temperature, so care should be taken when handling. It is irritating to the eyes, skin and respiratory tract and should be used with appropriate protective measures such as laboratory gloves, goggles and protective face masks. At the same time, avoid inhaling its vapor or dust, and keep away from ignition sources and oxidants. In the use or storage, should follow the appropriate safety procedures, and properly dispose of waste. It is best to use the compound under professional guidance.
Last Update：2024-04-10 22:29:15
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