| Weight | 192.302 g/mol |
|---|---|
| Formula | C13H20O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
beta-Damascone
damascone · alpha-damascone
639-99-6, 23726-91-2, 35044-68-9, 23726-91-2
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- Sigma-Aldrich - beta-Damascone40.00 - 587.00 USD
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- Synthesis of (R)-(+)- and (S)-(-)-.alpha.-damascone by tandem Grignard reaction-enantioselective protonation: evidence for the intermediacy of a chiral complex (Journal of the American Chemical Society, 1988)
- The Synthesis of Damascenone and Damascone and the possible mechanism of their formation from carotenoids (Helvetica Chimica Acta, 1973)
- Syntheses of the Enantiomers of Cyclogeranic Acid, Cyclocitral, and Damascone: Enantioselective protonation of enolates (Helvetica Chimica Acta, 1995)
- Efficient Synthesis of Enantiomerically Pure -Ionone from (R)- and (S)--Damascone (Helvetica Chimica Acta, 1992)
- Identification de la damascnone et de la -damascone dans le tabac Burley (Helvetica Chimica Acta, 1971)
- Synthesen der stereoisomeren ()--Damascone (Helvetica Chimica Acta, 1971)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - damascone
- alpha-damascone
-
SMILESCC=CC(=O)C1=C(CCCC1(C)C)C
-
InChIKeyBGTBFNDXYDYBEY-UHFFFAOYSA-N
- Pubchem - beta-Damascone
- Wikipedia - (E)--damascone
Damascones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascones belong to a family of chemicals known as rose ketones, which also includes damascenones and ionones. beta-Damascone is a contributor to the aroma of roses, despite its relatively low concentration, and is an important fragrance chemical used in perfumery.
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Synthesis
acetaldehyde
+
Reactant
(Wittig)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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beta-Damascone
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