| Weight | 238.415 g/mol |
|---|---|
| Formula | C16H30O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Muscone (541-91-3)
muskone · DL-3-methylcyclopentadecanone · 3-methylcyclopentadecanone
Score:
#786 in Neuroscience
,
#1464 in Biochemistry
,
#3458 in Biology
,
#4318 in Chemistry
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- Sigma-Aldrich - Search for Muscone
- Fisher Scientific - Search for Muscone
- TCI - Muscone94.00 - 328.00 USD
- CpRu(PN) Complex-Catalyzed Isomerization of Allylic Alcohols and Its Application to the Asymmetric Synthesis of Muscone (Journal of the American Chemical Society, 2005)
- Synthesis of (R)-(-)-muscone by an asymmetrically catalyzed macrocyclization of an .omega.-alkynal (Journal of the American Chemical Society, 1993)
- Synthesis of macrocycles by intramolecular ketophosphonate reactions. Stereoselective construction of the "left-wing" of carbomycin B and a synthesis of dl-muscone from oleic acid (Journal of Organic Chemistry, 1979)
- A three-carbon condensative expansion. Application to muscone (Journal of the American Chemical Society, 1980)
- Solid Phase Synthesis of Macrocycles by an Intramolecular Ketophosphonate Reaction. Synthesis of a (dl)-Muscone Library (Journal of the American Chemical Society, 1998)
- Psychological effects of musky compounds: Comparison of androstadienone with androstenol and muscone (Hormones and Behavior, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - muskone
- DL-3-methylcyclopentadecanone
- 3-methylcyclopentadecanone
-
SMILESCC1CCCCCCCCCCCCC(=O)C1
-
InChIKeyALHUZKCOMYUFRB-UHFFFAOYSA-N
- Pubchem - Muscone
- Wikipedia - (+/-)-muscone
Muscone is an organic compound that is the primary contributor to the odor of musk. The chemical structure of muscone was first elucidated by Lavoslav Ruika. It consists of a 15-membered ring ketone with one methyl substituent in the 3-position.
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