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Cuminaldehyde: Difference between revisions

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| OtherNames = Cuminaldehyde<br />''p''-Isopropylbenzaldehyde<br />4-Isopropylbenzaldehyde<br>Cuminal<br />Cumaldehyde
| OtherNames = Cuminaldehyde<br />''p''-Isopropylbenzaldehyde<br />4-Isopropylbenzaldehyde<br>Cuminal<br />Cumaldehyde
| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| SMILES = CC(C)C1=CC=C(C=O)C=C1
| SMILES = CC(C)c1ccc(C=O)cc1
| CASNo_Ref = {{cascite}}
| ChemSpiderID = 21106431
| InChI = 1/C10H12O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-8H,1-2H3
| InChIKey = WTWBUQJHJGUZCY-UHFFFAOYAP
| CASNo_Ref = {{cascite}}
| CASNo = 122-03-2
| CASNo = 122-03-2
| RTECS = CU7000000
| RTECS = CU7000000

Revision as of 09:26, 27 January 2010

Cuminaldehyde[1]
Cuminaldehyde
Names
IUPAC name
4-(1-Methylethyl)benzaldehyde
Other names
Cuminaldehyde
p-Isopropylbenzaldehyde
4-Isopropylbenzaldehyde
Cuminal
Cumaldehyde
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.004.107 Edit this at Wikidata
RTECS number
  • CU7000000
  • InChI=1/C10H12O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-8H,1-2H3
    Key: WTWBUQJHJGUZCY-UHFFFAOYAP
  • CC(C)c1ccc(C=O)cc1
Properties
C10H12O
Molar mass 148.205 g·mol−1
Appearance Colorless oil
Density 0.978 g/cm3
Boiling point 235 °C (455 °F; 508 K)
Insoluble
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability (yellow): no hazard codeSpecial hazards (white): no code
1
2
Flash point 93 °C
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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.

References

  1. ^ a b Merck Index, 11th Edition, 2623

See also