Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H14O2 |
| Molecular Weight | 178.2277 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)CCC1=CC=CC=C1
InChI
InChIKey=JAGZUIGGHGTFHO-UHFFFAOYSA-N
InChI=1S/C11H14O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
| Molecular Formula | C11H14O2 |
| Molecular Weight | 178.2277 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Volatile components in aqueous essence and fresh fruit of Cucumis melo cv. Athena (muskmelon) by GC-MS and GC-O. | 2001 Dec |
|
| Steryl and stanyl esters of fatty acids by solvent-free esterification and transesterification in vacuo using lipases from Rhizomucor miehei, Candida antarctica, and Carica papaya. | 2001 Nov |
|
| Pseudomonas cepacia lipase--mediated transesterification reactions of hydrocinnamates. | 2002 Aug |
|
| Potentiation of the ionotropic GABA receptor response by whiskey fragrance. | 2002 Nov 6 |
|
| Antifungal activity of extracts of some plants used in Brazilian traditional medicine against the pathogenic fungus Paracoccidioides brasiliensis. | 2010 Apr |
|
| Bioreduction of some common carbonylic compounds mediated by yeasts. | 2010 Jan-Feb |
|
| Phytochemical and pharmacological review of Lagenaria sicereria. | 2010 Oct |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:54:51 GMT 2023
by
admin
on
Fri Dec 15 18:54:51 GMT 2023
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| Record UNII |
58E9Z9V64D
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| Record Status |
Validated (UNII)
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CFR |
21 CFR 172.515
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JECFA EVALUATION |
ETHYL 3-PHENYLPROPIONATE
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178
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2021-28-5
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217-966-6
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