1-Phenyl-3-hexanone
1-Phenyl-3-hexanone
CAS: 29898-25-7
Molecular Formula: C12H16O
1-Phenyl-3-hexanone - Names and Identifiers
| Name | 1-Phenyl-3-hexanone |
| Synonyms | 1P3H 1-Phenylhexanone-3 1-Phenylhexan-3-one 1-PHENYL-3-HEXANONE 1-phenylhexan-3-one 1-Phenyl-3-hexanone 1-PHENYLHEXANE-3-ONE 3-Hexanone, 1-phenyl- 1-phenyl-3-Cyclohexanone B-PHENYLETHYL PROPYL KETONE |
| CAS | 29898-25-7 |
| EINECS | 249-937-9 |
| InChI | InChI=1/C12H16O/c1-2-6-12(13)10-9-11-7-4-3-5-8-11/h3-5,7-8H,2,6,9-10H2,1H3 |
1-Phenyl-3-hexanone - Physico-chemical Properties
| Molecular Formula | C12H16O |
| Molar Mass | 176.25 |
| Density | 0.9719 g/cm3(Temp: 40 °C) |
| Boling Point | 263 °C |
| Flash Point | 107°C |
| Vapor Presure | 0.012mmHg at 25°C |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.498 |
1-Phenyl-3-hexanone - Introduction
1-Phenyl-3-hexanone(1-Phenyl-3-hexanone) is an organic compound with the molecular formula C13H16O.
Nature:
1-Phenyl-3-hexanone is a colorless to pale yellow liquid. It has an aromatic phenyl group and a carbonyl (keto) group. It has a density of about 0.968 g/mL and a boiling point of about 260-262 ° C.
Use:
1-Phenyl-3-hexanone is widely used in organic synthesis reactions, such as in the manufacture of pharmaceutical and fragrance compounds, and can also be used as an intermediate in organic synthesis for the synthesis of other compounds.
Method:
1-Phenyl-3-hexanone is mainly prepared by acid-catalyzed reaction of acetylacetone and benzaldehyde. The reaction is usually carried out in absolute ethanol, and the catalyst is usually an acidic substance such as sulfuric acid.
Safety Information:
1-Phenyl-3-hexanone will not have serious fatal or toxic effects on the human body under normal use conditions. However, as an organic compound, it is flammable and should be avoided from exposure to open flames and high temperatures. Appropriate protective measures, such as gloves and goggles, should be worn during use. Store in a well-ventilated place away from ignition sources and avoid contact with strong oxidants and strong acids. In the case of accidental contact with skin or eyes, rinse immediately with plenty of water and seek medical help.
Nature:
1-Phenyl-3-hexanone is a colorless to pale yellow liquid. It has an aromatic phenyl group and a carbonyl (keto) group. It has a density of about 0.968 g/mL and a boiling point of about 260-262 ° C.
Use:
1-Phenyl-3-hexanone is widely used in organic synthesis reactions, such as in the manufacture of pharmaceutical and fragrance compounds, and can also be used as an intermediate in organic synthesis for the synthesis of other compounds.
Method:
1-Phenyl-3-hexanone is mainly prepared by acid-catalyzed reaction of acetylacetone and benzaldehyde. The reaction is usually carried out in absolute ethanol, and the catalyst is usually an acidic substance such as sulfuric acid.
Safety Information:
1-Phenyl-3-hexanone will not have serious fatal or toxic effects on the human body under normal use conditions. However, as an organic compound, it is flammable and should be avoided from exposure to open flames and high temperatures. Appropriate protective measures, such as gloves and goggles, should be worn during use. Store in a well-ventilated place away from ignition sources and avoid contact with strong oxidants and strong acids. In the case of accidental contact with skin or eyes, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 20:45:29
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