Chavibetol: Difference between revisions

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 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL259093 ;
ChemSpider	518422 ;
PubChem CID	596375;
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). verify (what is ?) Infobox references

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Revision as of 14:55, 1 November 2015

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]

^ 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.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Meta-eugenol, Good Scents Company

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

@@ Line 4: / Line 4: @@
 | verifiedrevid = 457284206
 | ImageFile = Chavibetol.svg
-| ImageSize = 200px
 | IUPACName = 2-Methoxy-5-(prop-2-en-1-yl)phenol
 | OtherNames = 5-Allylguaiacol; m-Eugenol; meta-Eugenol; 5-Allyl-2-methoxyphenol
-| Section1 = {{Chembox Identifiers
+|Section1={{Chembox Identifiers
 | CASNo = 501-19-9
-|  CASNo_Ref = {{cascite|changed|??}}
+| CASNo_Ref = {{cascite|changed|??}}
 | ChEMBL_Ref = {{ebicite|correct|EBI}}
 | ChEMBL = 259093
@@ Line 23: / Line 22: @@
 | StdInChIKey = NPBVQXIMTZKSBA-UHFFFAOYSA-N
  }}
-| Section2 = {{Chembox Properties
+|Section2={{Chembox Properties
-| C=10|H=12|O=2
+| C=10 | H=12 | O=2
-| ExactMass = 164.08372963 u
 | Appearance =
 | Density = 1.06 g/cm<sup>3</sup><ref>{{Cite journal | author = Hirao, Nenokichi | journal = Bulletin of the Chemical Society of Japan | year = 1936 | volume = 11 | pages = 179–184 | doi = 10.1246/bcsj.11.179 | title = Synthesis of 4-Hydroxy-3-Ethoxy-1-Allyl-Benzene from 4-Hydroxy-3 -Methoxy-1 -Allylbenzene (Eugenol) | issue = 3}}</ref>
 | MeltingPt =
 | BoilingPtC = 254
-|  Boiling_ref = <ref>''Traité élémentaire de chimie organique, Volume 1'', [[Marcellin Berthelot]], p 443</ref>
+| BoilingPt_ref = <ref>''Traité élémentaire de chimie organique, Volume 1'', [[Marcellin Berthelot]], p 443</ref>
 | Solubility =
  }}
-| Section3 = {{Chembox Hazards
+|Section3={{Chembox Hazards
 | MainHazards =
 | FlashPt =