Chavibetol

Chavibetol
Names
	Preferred 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 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL259093 ;
ChemSpider	518422 ;
PubChem CID	596375;
UNII	OE7NQ16G4D ;
CompTox Dashboard (EPA)	DTXSID70198206 ;
	InChI InChI=1S/C10H12O2/c1-3-4-8-5-6-10(12-2)9(11)7-8/h3,5-7,11H,1,4H2,2H3 Key: NPBVQXIMTZKSBA-UHFFFAOYSA-N ; 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	164.204 g·mol−1
Density	1.06 g/cm3
Boiling point	254 °C (489 °F; 527 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	(what is ?)
	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] and catatia.^[4] It is an aromatic compound with a spicy odor.^[5]

Uses[]

Decor, candle - Chemicals detected in substances or products (note that these chemicals may be absent from an 'ingredient list' for the product and thus unexpected, but have been detected in product testing studies)^[6]
Fragrance - Fragrances or odor agents, can be used in home products (cleaners, laundry products, air fresheners) or similar industrial products; usage indicated when known; more specific modifiers included when known.^[6]

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.
^ Niculau, Edenilson; Ribeiro, Leandro; Ansante, Thiago; Fernandes, João; Forim, Moacir; Vieira, Paulo; Vendramim, José; da Silva, Maria (2018). "Isolation of Chavibetol and Methyleugenol from Essential Oil of Pimenta pseudocaryophyllus by High Performance Liquid Chromatography". Molecules. 23 (11): 2909. doi:10.3390/molecules23112909. ISSN 1420-3049. PMC 6278253. PMID 30413007.
^ Meta-eugenol, Good Scents Company
^ ^a ^b PubChem. "Chavibetol". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-07-17.

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[1] 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.

[2] Traité élémentaire de chimie organique, Volume 1, Marcellin Berthelot, p 443

[3] Nigam, S. S.; Purohit, R. M. (1962). "Chemical examination of the essential oil of the leaves of Piper betel". Reichstoffe Aromen. 12: 185–190.

[NiculauRibeiro2018-4] Niculau, Edenilson; Ribeiro, Leandro; Ansante, Thiago; Fernandes, João; Forim, Moacir; Vieira, Paulo; Vendramim, José; da Silva, Maria (2018). "Isolation of Chavibetol and Methyleugenol from Essential Oil of Pimenta pseudocaryophyllus by High Performance Liquid Chromatography". Molecules. 23 (11): 2909. doi:10.3390/molecules23112909. ISSN 1420-3049. PMC 6278253. PMID 30413007.

[5] Meta-eugenol, Good Scents Company

[pubchem-6] PubChem. "Chavibetol". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-07-17.

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Chavibetol

Uses[]

See also[]

References[]