39751-07-0
adamantane-2,6-dione
CAS: 39751-07-0
Molecular Formula: C10H12O2
39751-07-0 - Names and Identifiers
| Name | adamantane-2,6-dione |
| Synonyms | 2,6-Dioxoadamantane adamantane-2,6-dione Tricyclo[3.3.1.13,7]decane-2,6-dione Tricyclo[3.3.1.13,7]decane-9,10-dione |
| CAS | 39751-07-0 |
39751-07-0 - Physico-chemical Properties
| Molecular Formula | C10H12O2 |
| Molar Mass | 164.2 |
| Density | 1.239 |
| Melting Point | 323-323.4 °C |
| Boling Point | 307℃ |
| Flash Point | 115℃ |
| Storage Condition | Sealed in dry,Room Temperature |
39751-07-0 - Introduction
adamantane-2,6-dione is an organic compound with a chemical formula of calloc H. It is a diketone derivative of adamantane in the form of a white crystalline solid.
adamantane-2,6-dione is mainly used as an intermediate and raw material for organic synthesis. It can be used to prepare a variety of organic compounds, such as drugs, dyes, fragrances and pesticides. It can also be used as a ligand for chemical reagents and catalysts.
adamantane-2, the preparation of 6-dione is usually accomplished by a two-step reaction. First, adamantane reacts with nitric acid to form nitroadamantane, and then adamantane-2,6-dione, is obtained by reduction and carboxylation.
adamantane-2,6-dione is relatively stable under normal conditions, but it is combustible and must avoid contact with strong oxidants. Appropriate protective measures should be taken during operation, including gloves, goggles and protective clothing. In addition, care should be taken to prevent its inhalation and contact with the skin. During storage and handling, safe operating instructions should be followed.
In General, adamantane-2,6-dione is an important organic compound with a wide range of applications and plays an important role in organic synthesis and chemical research.
adamantane-2,6-dione is mainly used as an intermediate and raw material for organic synthesis. It can be used to prepare a variety of organic compounds, such as drugs, dyes, fragrances and pesticides. It can also be used as a ligand for chemical reagents and catalysts.
adamantane-2, the preparation of 6-dione is usually accomplished by a two-step reaction. First, adamantane reacts with nitric acid to form nitroadamantane, and then adamantane-2,6-dione, is obtained by reduction and carboxylation.
adamantane-2,6-dione is relatively stable under normal conditions, but it is combustible and must avoid contact with strong oxidants. Appropriate protective measures should be taken during operation, including gloves, goggles and protective clothing. In addition, care should be taken to prevent its inhalation and contact with the skin. During storage and handling, safe operating instructions should be followed.
In General, adamantane-2,6-dione is an important organic compound with a wide range of applications and plays an important role in organic synthesis and chemical research.
Last Update：2024-04-09 21:32:46
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