| Weight | 130.146 g/mol |
|---|---|
| Formula | C9H6O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Phenylpropiolaldehyde (2579-22-8)
phenylpropynal
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- Phenylpropynal, a specific, irreversible, non-beta-lactam inhibitor of beta-lactamases. (Journal of Biological Chemistry, 1980)
- Self-Assembling 3-[2-Pyridylamino(phenyl)methyl]imidazo-[1,2-a]pyridine from phenylpropynal and 2-aminopyridine (Russian Journal of Organic Chemistry, 2008)
- General and Direct Synthesis of Indolizine-1-carbaldehydes by 1,3-Dipolar Cycloaddition of Phenylpropiolaldehyde with Pyridinium Ylides (European Journal of Organic Chemistry, 2016)
- Reactions of Phenylpropynal N-tert-Butylimine with 4-Amino-3-mercapto-1,2,4-triazole Derivatives (Russian Journal of General Chemistry, 2005)
- Reaction of diphenyldiazomethane with phenylpropiolaldehyde (Chemistry of Heterocyclic Compounds, 1978)
- 1H nuclear magnetic resonance and molecular orbital estimates of the internal rotational barrier in phenylpropynal in solution and in the vapor (Canadian Journal of Chemistry, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenylpropynal
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SMILESC1=CC=C(C=C1)C#CC=O
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InChIKeyIDASOVSVRKONFS-UHFFFAOYSA-N
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Phenylpropiolaldehyde
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