| Weight | 150.221 g/mol |
|---|---|
| Formula | C10H14O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Myrtenal (564-94-3, 23727-16-4)
Score:
#1680 in Physics
,
#1940 in Biochemistry
,
#5187 in Chemistry
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- Methyl salicylate and ()-(1R,5S)-myrtenal are plant-derived repellents for black bean aphid,Aphis fabae Scop. (Homoptera: Aphididae) (Journal of Chemical Ecology, 1994)
- Terpenoid biotransformation in mammals. V. Metabolism of (+)-citronellal, (+-)-7-hydroxycitronellal, citral, (-)-perillaldehyde, (-)-myrtenal, cuminaldehyde, thujone, and (+-)-carvone in rabbits. (Xenobiotica, 1989)
- The search for tolerant Lewis acid catalysts. Part 1: Chiral silicon Lewis acids derived from (-)-myrtenal (Tetrahedron Letters, 2000)
- Absolute configuration of ()-myrtenal by vibrational circular dichroism (Phytochemistry, 2010)
- Chiral separation membranes from modified polysulfone having myrtenal-derived terpenoid side groups (European Polymer Journal, 2006)
- Enantioselective synthesis of 1-alkyl-substituted 1-phenyl-1,2-ethanediols using a myrtenal-derived chiral auxiliary (Tetrahedron-asymmetry, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1(C2CC=C(C1C2)C=O)C
-
InChIKeyKMRMUZKLFIEVAO-UHFFFAOYSA-N
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