Misplaced Pages

Ethyl cinnamate

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by CheMoBot (talk | contribs) at 16:18, 12 January 2011 (Updating {{chembox}} (no changed fields - added verified revid - updated 'ChEMBL_Ref') per Chem/Drugbox validation (report errors or [[user talk:CheMoBot|). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 16:18, 12 January 2011 by CheMoBot (talk | contribs) (Updating {{chembox}} (no changed fields - added verified revid - updated 'ChEMBL_Ref') per Chem/Drugbox validation (report errors or [[user talk:CheMoBot|)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed.
Find sources: "Ethyl cinnamate" – news · newspapers · books · scholar · JSTOR (July 2009) (Learn how and when to remove this message)
Ethyl cinnamate
Skeletal formula
Ball-and-stick model
Names
IUPAC name Ethyl 3-phenylprop-2-enoate
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.002.822 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+Key: KBEBGUQPQBELIU-CMDGGOBGSA-N
  • InChI=1/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+Key: KBEBGUQPQBELIU-CMDGGOBGBD
SMILES
  • CCOC(=O)/C=C/c1ccccc1
Properties
Chemical formula C11H12O2
Molar mass 176.21 g/mol
Density 1.046 g/cm
Melting point 6.5-8 °C
Boiling point 271 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Ethyl cinnamate is the ester of cinnamic acid and ethanol. It is present in the essential oil of cinnamon ; pure ethyl cinnamate has a "fruity and balsamic odor, reminiscent of cinnamon with an amber note" .
The p-methoxy substitute is reported to be a monoamine oxidase inhibitor.

List of plants that contain the chemical

Toxicology

This section is empty. You can help by adding to it. (September 2009)

Notes and references

This article has an unclear citation style. The references used may be made clearer with a different or consistent style of citation and footnoting. (September 2007) (Learn how and when to remove this message)
  1. Budavari, Susan (2001). "Merck Index 13th Ed". Merck & co., Inc.
  2. Noro T, Miyase T, Kuroyanagi M, Ueno A, Fukushima S. (1983). "Monoamine oxidase inhibitor from the rhizomes of Kaempferia galanga L.". Chem Pharm Bull (Tokyo). 31 (8): 2708–11. PMID 6652816.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. Wong, K. C.; Ong, K. S.; Lim, C. L.; et al. (2006). "Compositon of the essential oil of rhizomes of kaempferia galanga L.". Flavour and Fragrance Journal. 7 (5): 263–266. doi:10.1002/ffj.2730070506. {{cite journal}}: |access-date= requires |url= (help); Cite has empty unknown parameter: |coauthors= (help); Explicit use of et al. in: |first= (help)
  4. Othman, R.; Ibrahim, H; Mohd, MA; Mustafa, MR; Awang, K; et al. (2006). "Bioassay-guided isolation of a vasorelaxant active compound from Kaempferia galanga L.". Phytomedicine. 13 (1–2): 61–66. doi:10.1016/j.phymed.2004.07.004. PMID 16360934. {{cite journal}}: |access-date= requires |url= (help); Cite has empty unknown parameter: |coauthors= (help); Explicit use of et al. in: |first= (help)


Stub icon

This article about an ester is a stub. You can help Misplaced Pages by expanding it.

Categories: