Farnesylacetone - CAS 762-29-8
Catalog: |
BB035531 |
Product Name: |
Farnesylacetone |
CAS: |
762-29-8 |
Synonyms: |
6,10,14-trimethylpentadeca-5,9,13-trien-2-one |
IUPAC Name: | 6,10,14-trimethylpentadeca-5,9,13-trien-2-one |
Description: | Farnesylacetone (CAS# 762-29-8) is an intermediate in the synthesis of intermediates in the biosynthesis of carotenoids. |
Molecular Weight: | 262.43 |
Molecular Formula: | C18H30O |
Canonical SMILES: | CC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C |
InChI: | InChI=1S/C18H30O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h9,11,13H,6-8,10,12,14H2,1-5H3 |
InChI Key: | LTUMRKDLVGQMJU-UHFFFAOYSA-N |
Boiling Point: | 334.71 °C (EPI 4.0) |
Flash Point: | 140.4°C |
Purity: | 95.0 % |
Density: | 0.88 g/cm3 |
Solubility: | Insoluble in water; soluble in alcohol. |
Appearance: | Colorless liquid |
Storage: | Store tightly sealed under inert gas in a cool, well-ventilated area. |
LogP: | 5.77480 |
Refractive Index: | 1.476 : 1.486 at 20 deg C |
Publication Number | Title | Priority Date |
CN-112956728-A | Electronic atomized liquid based on female warmth and preparation method thereof | 20210310 |
US-2021100242-A1 | Formulations for control and repellency of biting arthropods | 20191008 |
US-2021100245-A1 | Synergistic formulations for control and repellency of biting arthropods | 20191008 |
WO-2021071896-A1 | Synergistic formulations for control and repellency of biting arthropods | 20191008 |
WO-2021071898-A1 | Formulations for control and repellency of biting arthropods | 20191008 |
PMID | Publication Date | Title | Journal |
20569134 | 20100101 | Constituents of the essential oil of Suregada zanzibariensis leaves are repellent to the mosquito, Anopheles gambiae s.s | Journal of insect science (Online) |
19186019 | 20090405 | Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry | Journal of pharmaceutical and biomedical analysis |
19006667 | 20081215 | Vasodilatation effect of farnesylacetones, active constituents of Sargassum siliquastrum, on the basilar and carotid arteries of rabbits | Bioorganic & medicinal chemistry letters |
18687007 | 20080801 | Linear and cyclic C18 terpenoids from the southern Australian marine brown alga Cystophora moniliformis | Journal of natural products |
16458520 | 20060515 | Isolation and characterization of a monoamine oxidase B selective inhibitor from tobacco smoke | Bioorganic & medicinal chemistry |
Complexity: | 352 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 262.229665576 |
Formal Charge: | 0 |
Heavy Atom Count: | 19 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 262.229665576 |
Rotatable Bond Count: | 9 |
Topological Polar Surface Area: | 17.1 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 2 |
XLogP3: | 5.6 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS