Weight | 98.145 g/mol |
---|---|
Formula | C6H10O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
cis-3-Hexenal (6789-80-6)
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- Sigma-Aldrich - cis-3-Hexenal200.00 - 458.00 USD
- Fisher Scientific - Search for cis-3-Hexenal
- TCI - Search for cis-3-Hexenal
- Rate constants for the gasphase reactions of cis3Hexen1ol, cis3Hexenylacetate, trans2Hexenal, and Linalool with OH and NO3 radicals and O3 at 296 2 K, and OH radical formation yields from the O3 reactions (International Journal of Chemical Kinetics, 1995)
- Formation of cis-3-hexenal, trans-2-hexenal and cis-3-hexenol in macerated Thea sinensis leaves (Phytochemistry, 1973)
- 3-cis-hexenal, the Green reversion flavor of soybean oil (Journal of the American Oil Chemists' Society, 1961)
- Distribution of an enzyme system producing cis-3-hexenal and n-hexanal from linolenic and linoleic acids in some plants (Phytochemistry, 1978)
- Enzyme system catalyzing formation of cis-3-hexenal and n-hexanal from linolenic and linoleic acids in Japanese silver (Farfugium iaponicum Kitamura) leaves (Plant and Cell Physiology, 1977)
- Seasonal changes in activity of the enzyme system producing cis-3-hexenal and n-hexanal from linolenic and linoleic acids in tea leaves (Plant and Cell Physiology, 1977)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC=CCC=O
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InChIKeyGXANMBISFKBPEX-UHFFFAOYSA-N
- Pubchem - cis-3-Hexenal
- Wikipedia - (3Z)-3-hexenal
cis-3-Hexenal, also known as (Z)-3-hexenal and leaf aldehyde, is colorless liquid and an aroma compound with an intense odor of freshly cut grass and leaves. It is one of the major volatile compounds in ripe tomatoes. It is produced in small amounts by most plants and it acts as an attractant to many predatory insects.
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