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| Description: | 1-Octen-3-ol (CAS# 3391-86-4) is one of the volatiles responsible for mold`s odor. It can be used in combination with carbon dioxide to attract insects in order to kill them. In animal study, 1-Octen-3-ol has been shown to interfere with dopamine transport in the brain of fruit flies, so it might be an environmental agent involved in parkinsonism. |
| Molecular Weight: | 128.21 |
| Molecular Formula: | C8H16O |
| Canonical SMILES: | CCCCCC(C=C)O |
| InChI: | InChI=1S/C8H16O/c1-3-5-6-7-8(9)4-2/h4,8-9H,2-3,5-7H2,1H3 |
| InChI Key: | VSMOENVRRABVKN-UHFFFAOYSA-N |
| Boiling Point: | 180.31 ℃ (EPI 4.0) |
| Melting Point: | -49°C |
| Flash Point: | 68°C |
| Purity: | 98.0 % |
| Density: | 0.837 g/cm3 |
| Solubility: | Insoluble in water; soluble in alcohol. |
| Appearance: | Colorless to pale yellow liquid |
| Storage: | Store tightly sealed under inert gas in a cool, well-ventilated area. |
| MDL: | MFCD00004589 |
| LogP: | 2.11360 |
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Medicinal chemistry and drug research require diverse chemical components to meet strict requirements not only in terms of physical and chemical properties but also in terms of chemical reactivity.
Medicinal chemistry and drug research require diverse chemical components to meet strict requirements not only in terms of physical and chemical properties but also in terms of chemical reactivity.
The chemists use the 'build–couple–pair' strategy of organic synthesis, which entails preparing molecular building blocks that contain several chemical groups.
The chemical building block (CBB) is a molecule which can be converted to various secondary chemicals and intermediates, and, in turn, into a broad range of different downstream uses.
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