Chavibetol

Chavibetol
Names

IUPAC name 2-Methoxy-5-(prop-2-en-1-yl)phenol
Other names 5-Allylguaiacol; m-Eugenol; meta-Eugenol; 5-Allyl-2-methoxyphenol
Identifiers
CAS Number	501-19-9^N
3D model (JSmol)	Interactive image
ChemSpider	518422^Y
PubChem CID	596375
InChI InChI=1S/C10H12O2/c1-3-4-8-5-6-10(12-2)9(11)7-8/h3,5-7,11H,1,4H2,2H3^Y Key: NPBVQXIMTZKSBA-UHFFFAOYSA-N^Y InChI=1/C10H12O2/c1-3-4-8-5-6-10(12-2)9(11)7-8/h3,5-7,11H,1,4H2,2H3 Key: NPBVQXIMTZKSBA-UHFFFAOYAR
SMILES Oc1cc(ccc1OC)C\C=C
Properties
Chemical formula	C₁₀H₁₂O₂
Molar mass	164.20 g·mol⁻¹
Density	1.06 g/cm³^[1]
Boiling point	254 °C (489 °F; 527 K)^[2]
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

Chavibetol is an organic chemical compound of the phenylpropanoid class. It is one of the primary constituents of the essential oil from the leaves of the betel plant (Piper betel).^[3] It is an aromatic compound with a spicy odor.^[4]

References

↑ Hirao, Nenokichi (1936). "Synthesis of 4-Hydroxy-3-Ethoxy-1-Allyl-Benzene from 4-Hydroxy-3 -Methoxy-1 -Allylbenzene (Eugenol)". Bulletin of the Chemical Society of Japan. 11 (3): 179–184. doi:10.1246/bcsj.11.179.
↑ Traité élémentaire de chimie organique, Volume 1, Marcellin Berthelot, p 443
↑ Nigam, S. S.; Purohit, R. M. (1962). "Chemical examination of the essential oil of the leaves of Piper betel". Reichstoffe Aromen. 12: 185–190.
↑ Meta-eugenol, Good Scents Company

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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