CAS 7787-20-4|(-)-Fenchone
Introduction：Basic information about CAS 7787-20-4|(-)-Fenchone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | (-)-Fenchone | ||
|---|---|---|---|
| CAS Number | 7787-20-4 | Molecular Weight | 152.233 |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 193.5±0.0 °C at 760 mmHg |
| Molecular Formula | C10H16O | Melting Point | 5ºC |
| MSDS | ChineseUSA | Flash Point | 52.8±0.0 °C |
| Symbol | GHS02 | Signal Word | Warning |
Names
| Name | (1R,4S)-fenchone |
|---|---|
| Synonym | More Synonyms |
(-)-Fenchone BiologicalActivity
| Description | (-)-Fenchone, a bicyclic monoterpene, is widely distributed in plants and found in essential oils from Thuja occidentalis. (-)-Fenchone is oxidized to 6-endo-hydroxyfenchone, 6-exo-hydroxyfenchone and 10-hydroxyfenchone derivatives by CYP2A6 and CYP2B6 in human liver microsomes with CYP2A6 playing a more important role than CYP2B6[1]. |
|---|---|
| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
| References | [1]. Miyazawa M, et al. Metabolism of (-)-fenchone by CYP2A6 and CYP2B6 in human liver microsomes. Xenobiotica. 2007;37(2):194-204. |
Chemical & Physical Properties
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 193.5±0.0 °C at 760 mmHg |
| Melting Point | 5ºC |
| Molecular Formula | C10H16O |
| Molecular Weight | 152.233 |
| Flash Point | 52.8±0.0 °C |
| Exact Mass | 152.120117 |
| PSA | 17.07000 |
| LogP | 2.13 |
| Vapour Pressure | 0.5±0.3 mmHg at 25°C |
| Index of Refraction | 1.485 |
| InChIKey | LHXDLQBQYFFVNW-OIBJUYFYSA-N |
| SMILES | CC12CCC(C1)C(C)(C)C2=O |
| Storage condition | Flammables area |
Safety Information
| Symbol | GHS02 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H226 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Risk Phrases | R10 |
| Safety Phrases | S16 |
| RIDADR | UN 1224 3/PG 3 |
| WGK Germany | 3 |
| RTECS | RB7875000 |
| Packaging Group | III |
| Hazard Class | 3.0 |
Articles25
More Articles| [Chemical composition of essential oil obtained from Romanian fennel fruits]. Rev. Med. Chir. Soc. Med. Nat. Iasi. 115(2) , 590-4, (2011) For therapeutical purposes, fennel (Foeniculum vulgare Mill.), an important aromatic plant, is used for its expectorant, antispasmodic, carminative and diuretic properties. The chemical composition, e... | |
| Biosynthesis of monoterpenes: conversion of the acyclic precursors geranyl pyrophosphate and neryl pyrophosphate to the rearranged monoterpenes fenchol and fenchone by a soluble enzyme preparation from fennel (Foeniculum vulgare). Arch. Biochem. Biophys. 200(2) , 524-33, (1980) | |
| Kinetics and mechanisms of the tropospheric reactions of menthol, borneol, fenchol, camphor, and fenchone with hydroxyl radicals (OH) and chlorine atoms (Cl). J. Phys. Chem. A 116(16) , 4097-107, (2012) Relative kinetic techniques have been used to measure the rate coefficients for the reactions of oxygenated terpenes (menthol, borneol, fenchol, camphor, and fenchone) and cyclohexanol with hydroxyl r... |
Synonyms
| (1R,4S)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one |
| EINECS 232-107-5 |
| MFCD00151104 |
| (1R)-(-)-Fenchone |
| 2-Norbornanone, 1,3,3-trimethyl-, (1R,4S)-(+)- |
| (-)-1,3,3-Trimethyl-2-norbornanone |
| Bicyclo[2.2.1]heptan-2-one, 1,3,3-trimethyl-, (1R,4S)- |
| (+)-FENCHONE |
| (1R,4S)-fenchone |
