2094-74-8
tricyclo[3.3.1.13,7<|sup>]decane-1-carbaldehyde
CAS: 2094-74-8
Molecular Formula: C11H16O
2094-74-8 - Names and Identifiers
| Name | tricyclo[3.3.1.13,7<|sup>]decane-1-carbaldehyde |
| Synonyms | 1-AdaMantane ADAMANTANE-1-ALDEHYDE Adamantane-1-carbaldehyde 1-Adamantylcarboxaldehyde 1-Adamantane Carboxaldehyde Adamantane-1-carboxaldehyde 1-ADAMANTANE CARBOXALDEHYDE 1-AdaMantanecarboxaldehyde (7CI,8CI) Tricyclo[3.3.1.13,7]decane-1-carboxaldehyde |
| CAS | 2094-74-8 |
| InChI | InChI=1/C11H16O/c12-7-11-4-8-1-9(5-11)3-10(2-8)6-11/h7-10H,1-6H2 |
2094-74-8 - Physico-chemical Properties
| Molecular Formula | C11H16O |
| Molar Mass | 164.24 |
| Density | 1.166 |
| Melting Point | 189-198 °C |
| Boling Point | 239℃ |
| Flash Point | 82℃ |
| Vapor Presure | 0.041mmHg at 25°C |
| Storage Condition | -20℃ |
| Refractive Index | 1.609 |
| MDL | MFCD12031698 |
2094-74-8 - Introduction
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde is an organic compound with the chemical formula C6H5CH2CHO. It is a colorless liquid with a special aromatic smell. The following is a description of the nature, use, preparation and safety information of the tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde:
Nature:
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde is a liquid that is insoluble in water and soluble in organic solvents. It has a low boiling point and ignition point, volatile, sensitive to air.
Use:
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde are mainly used as intermediates in organic synthesis reactions. It can be used as a raw material for the preparation of chemicals such as pharmaceutical synthesis, dyes, fragrances and pesticides. In addition, it can also be used for surface treatment, metal corrosion inhibition, plastic processing and paint coatings.
Method:
tricyclo[3.3.1.13,7<| sup>] The synthesis of decane-1-carbaldehyde is generally obtained by the catalytic reduction reaction of benzyl bromide and hydrogen. First, benzyl bromide is reacted with a basic hydride to produce a 1-adamantyl compound. Then, the adamantyl compound is reduced to tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde by Hydrogen Catalytic reduction reaction under the action of a catalyst.
Safety Information:
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde need to pay attention to safety protection measures during use. It is irritating and corrosive and may cause irritation of the eyes, skin and respiratory tract. Personal protective equipment such as goggles, gloves and masks should be worn during use. Avoid breathing gas and contact with skin. During the operation, it should be well ventilated and avoid contact with oxidants and other substances. If contact occurs, rinse quickly with plenty of water and seek medical attention.
Nature:
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde is a liquid that is insoluble in water and soluble in organic solvents. It has a low boiling point and ignition point, volatile, sensitive to air.
Use:
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde are mainly used as intermediates in organic synthesis reactions. It can be used as a raw material for the preparation of chemicals such as pharmaceutical synthesis, dyes, fragrances and pesticides. In addition, it can also be used for surface treatment, metal corrosion inhibition, plastic processing and paint coatings.
Method:
tricyclo[3.3.1.13,7<| sup>] The synthesis of decane-1-carbaldehyde is generally obtained by the catalytic reduction reaction of benzyl bromide and hydrogen. First, benzyl bromide is reacted with a basic hydride to produce a 1-adamantyl compound. Then, the adamantyl compound is reduced to tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde by Hydrogen Catalytic reduction reaction under the action of a catalyst.
Safety Information:
tricyclo[3.3.1.13,7<| sup>]decane-1-carbaldehyde need to pay attention to safety protection measures during use. It is irritating and corrosive and may cause irritation of the eyes, skin and respiratory tract. Personal protective equipment such as goggles, gloves and masks should be worn during use. Avoid breathing gas and contact with skin. During the operation, it should be well ventilated and avoid contact with oxidants and other substances. If contact occurs, rinse quickly with plenty of water and seek medical attention.
Last Update：2024-04-09 21:01:54
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View History
2094-74-8
Hispidine
1-tert-butyl 4-ethyl 3,3-difluoropiperidine-1,4-dicarboxylate
RADIUM228
17755-10-1
1,3-DIOXOLANE-4-CARBOXALDEHYDE, 2,2-DIMETHYL-, (R)-
2,2′-(oxydimethanediyl)bis(5-nitro-1H-benzimidazole)
1-(9H-fluoren-2-yl)ethan-1-one
9-DEMETHYL FR-901235
5-NIPA DME
Hispidine
1-tert-butyl 4-ethyl 3,3-difluoropiperidine-1,4-dicarboxylate
RADIUM228
17755-10-1
1,3-DIOXOLANE-4-CARBOXALDEHYDE, 2,2-DIMETHYL-, (R)-
2,2′-(oxydimethanediyl)bis(5-nitro-1H-benzimidazole)
1-(9H-fluoren-2-yl)ethan-1-one
9-DEMETHYL FR-901235
5-NIPA DME