| Weight | 134.178 g/mol |
|---|---|
| Formula | C9H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
2-Phenylpropanal (93-53-8)
hydratropic aldehyde · 2-phenylpropenal
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- Synthesis and in vitro reactivity of 3-carbamoyl-2-phenylpropionaldehyde and 2-phenylpropenal: putative reactive metabolites of felbamate. (Chemical Research in Toxicology, 1996)
- The loss of C2H2O and of C3H4O from the molecular ions of 3-phenylpropanal as studied by field ionization kinetics. Isomerization of the molecular ions of 3-phenyl-2-propen-1-ol (Journal of the American Chemical Society, 1978)
- Cram Selectivity in the Reaction of 2-Phenylpropanal with Alkyllithium Reagents: Myth and Reality (Tetrahedron, 1992)
- The Stereochemistry of Nucleophilic Addition. V. The Reformatsky Reaction of 2-Phenylpropanal with Methyl -Bromopropionate (Bulletin of the Chemical Society of Japan, 1972)
- Role of glutathione S-transferases A1-1, M1-1, and P1-1 in the detoxification of 2-phenylpropenal, a reactive felbamate metabolite. (Chemical Research in Toxicology, 2001)
- Investigating the Role of 2-Phenylpropenal in Felbamate-Induced Idiosyncratic Drug Reactions (Chemical Research in Toxicology, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - hydratropic aldehyde
- 2-phenylpropenal
-
SMILESCC(C=O)C1=CC=CC=C1
-
InChIKeyIQVAERDLDAZARL-UHFFFAOYSA-N
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2-Phenylpropanal
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