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Ethyl cinnamate
Ethyl cinnamate
IUPAC name
Identifiers
CAS number 103-36-6 Yes check.svgY
SMILES
Properties
Molecular formula C11H12O2
Molar mass 176.21 g/mol
Density 1.046 g/cm3
Melting point

6.5-8 °C

Boiling point

271 °C

 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

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" [1].
The p-methoxy substitute is reported to be a monoamine oxidase inhibitor[2].

List of plants that contain the chemical

Toxicology

Notes & References

  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.  
  3. ^ Wong, K. C. 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.  
  4. ^ Othman, R. 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.  
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Ethyl cinnamate
Identifiers
CAS number 103-36-6 Y
PubChem 637758
ChemSpider 553344
UNII C023P3M5JJ Y
SMILES
InChI
InChI key
Properties
Molecular formula C11H12O2
Molar mass 176.21 g/mol
Density 1.046 g/cm3
Melting point

6.5-8 °C

Boiling point

271 °C

 Y (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Ethyl cinnamate is the ester of cinnamic acid and ethanol. It is present in the essential oil of cinnamon[citation needed]; pure ethyl cinnamate has a "fruity and balsamic odor, reminiscent of cinnamon with an amber note" [1].
The p-methoxy substitute is reported to be a monoamine oxidase inhibitor[2].

List of plants that contain the chemical

Toxicology

Notes and references

  1. ^ Budavari, Susan (2001). [Expression error: Unexpected < operator "Merck Index 13th Ed."]. Merck & co., Inc. 
  2. ^ Noro T, Miyase T, Kuroyanagi M, Ueno A, Fukushima S. (1983). [Expression error: Unexpected < operator "Monoamine oxidase inhibitor from the rhizomes of Kaempferia galanga L."]. Chem Pharm Bull (Tokyo). 31 (8): 2708–11. PMID 6652816. 
  3. ^ Wong, K. C. et al.; Ong, K. S.; Lim, C. L. (2006). [Expression error: Unexpected < operator "Compositon of the essential oil of rhizomes of kaempferia galanga L."]. Flavour and Fragrance Journal 7 (5): 263–266. doi:10.1002/ffj.2730070506. 
  4. ^ Othman, R. et al.; Ibrahim, H; Mohd, MA; Mustafa, MR; Awang, K (2006). [Expression error: Unexpected < operator "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. 

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