| Weight | 150.133 g/mol |
|---|---|
| Formula | C8H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
PIPERONAL (120-57-0)
heliotropin · 3,4-methylenedioxybenzaldehyde · heliotrin
Score:
#5 in Inorganic chemistry
,
#2713 in Chemistry
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- Half-sandwich rutheniumarene complexes with thiosemicarbazones: Synthesis and biological evaluation of [(6-p-cymene)Ru(piperonal thiosemicarbazones)Cl]Cl complexes (Journal of Inorganic Biochemistry, 2011)
- Substitution Reactions of Specifically Ortho-Metalated Piperonal Cyclohexylimine (Journal of Organic Chemistry, 1976)
- Piperonal as electrophile in the Baylis-Hillman reaction. A synthesis of hydroxy--piperonyl--butyrolactone derivative (Tetrahedron Letters, 1998)
- Concentrations of nine alkenylbenzenes, coumarin, piperonal and pulegone in Indian bidi cigarette tobacco. (Food and Chemical Toxicology, 2003)
- High Selectivity in the Oxidation of Mandelic Acid Derivatives and in O-Methylation of Protocatechualdehyde: New Processes for Synthesis of Vanillin, iso-Vanillin, and Heliotropin (Organic Process Research & Development, 2000)
- Highly stereoselective PictetSpengler reaction of d-tryptophan methyl ester with piperonal: convenient syntheses of Cialis (Tadalafil), 12a-epi-Cialis, and their deuterated analogues (Tetrahedron-asymmetry, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - heliotropin
- 3,4-methylenedioxybenzaldehyde
- heliotrin
-
SMILESC1OC2=C(O1)C=C(C=C2)C=O
-
InChIKeySATCULPHIDQDRE-UHFFFAOYSA-N
- Pubchem - PIPERONAL
- Wikipedia - piperonal
Piperonal, also known as heliotropin, is an organic compound which is commonly found in fragrances and flavors. The molecule is structurally related to other aromatic aldehydes such as benzaldehyde and vanillin.
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PIPERONAL
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