Cuminaldehyde[1] | |
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4-(1-Methylethyl)benzaldehyde |
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Other names
Cuminaldehyde |
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Identifiers | |
CAS number | 122-03-2 |
ChemSpider | 21106431 |
UNII | O0893NC35F |
KEGG | C06577 |
ChEMBL | CHEMBL161577 |
RTECS number | CU7000000 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C10H12O |
Molar mass | 148.2 g mol−1 |
Appearance | Colorless oil |
Density | 0.978 g/cm3 |
Boiling point |
235 °C, 508 K, 455 °F |
Solubility in water | Insoluble |
Hazards | |
R-phrases | R22 |
S-phrases | S36/37 |
NFPA 704 |
2
1
0
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Flash point | 93 °C |
Related compounds | |
Related compounds | Benzaldehyde Cumene Cuminol |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Cuminaldehyde, or 4-isopropylbenzaldehyde, is a natural organic compound with the molecular formula C10H12O. It is a benzaldehyde with an isopropyl group substituted in the 4-position.
Cuminaldehyde is a constituent of the essential oils of eucalyptus, myrrh, cassia, cumin and others.[1] It has a pleasant smell and contributes to the aroma of these oils. It is used commercially in perfumes and other cosmetics.
Cuminaldehyde can be prepared synthetically by the reduction of 4-isopropylbenzoyl chloride or by the formylation of cumene.
The thiosemicarbazone of cuminaldehyde has antiviral properties.