Chavicol

Chavicol
Names


Preferred IUPAC name 4-(Prop-2-en-1-yl)phenol
Other names 4-Allylphenol
Identifiers
CAS Number	501-92-8^N
3D model (Jmol)	Interactive image
ChEBI	CHEBI:50158^Y
ChEMBL	ChEMBL108862^Y
ChemSpider	21105856^Y
ECHA InfoCard	100.007.209
UNII	Q5ER4K6969^Y
InChI InChI=1S/C9H10O/c1-2-3-8-4-6-9(10)7-5-8/h2,4-7,10H,1,3H2^Y Key: RGIBXDHONMXTLI-UHFFFAOYSA-N^Y InChI=1/C9H10O/c1-2-3-8-4-6-9(10)7-5-8/h2,4-7,10H,1,3H2 Key: RGIBXDHONMXTLI-UHFFFAOYAI
SMILES C=CCC1=CC=C(C=C1)O
Properties
Chemical formula	C₉H₁₀O
Molar mass	134.18 g/mol
Density	1.020 g/cm³
Melting point	16 °C (61 °F; 289 K)
Boiling point	238 °C (460 °F; 511 K) (123 °C at 16 mmHg)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Chavicol, or p-allylphenol, is a natural phenylpropene, a type of organic compound.^[1] Its chemical structure consists of a benzene ring substituted with a hydroxy group and a propenyl group. It is a colorless liquid found together with terpenes in betel oil.

Properties

Chavicol is miscible with alcohol, ether, and chloroform.

Uses

Chavicol is used as an odorant in perfumery.

References

↑ Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5.

Types of phenylpropenes

Phenylpropenes	Anethole Apiole Asaricin Asarone Carpacin Chavibetol Chavicol Croweacin Dillapiole Elemicin Estragole Eugenol Exalatacin Isoapiole Isodillapiole Isoeugenol Isomyristicin Isosafrole Methyl eugenol Myristicin Nothosmyrnol Osmorhizole Safrole

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Chavicol

Properties

Uses

See also

References