Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.2112 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)CC(=O)C1=CC=CC=C1
InChI
InChIKey=GKKZMYDNDDMXSE-UHFFFAOYSA-N
InChI=1S/C11H12O3/c1-2-14-11(13)8-10(12)9-6-4-3-5-7-9/h3-7H,2,8H2,1H3
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.2112 |
| 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 |
|---|---|---|
| Determination of acidity constants of enolisable compounds by capillary electrophoresis. | 2004 Oct |
|
| A novel manganese(III) acetate mediated reaction between 2-benzoyl-1,4-naphthoquinones and 1,3-dicarbonyl compounds. | 2006 Mar 21 |
|
| Enantioselective reduction of ketones with borane catalyzed by tridentate amino alcohols derived from salicylaldehyde. | 2007 Feb |
|
| 4-Amino-2-methyl-quinoline monohydrate. | 2008 May 10 |
|
| Application of comparative proteome analysis to reveal influence of cultivation conditions on asymmetric bioreduction of beta-keto ester by Saccharomyces cerevisiae. | 2008 Oct |
|
| Free radical reaction between 2-benzoyl-1,4-benzoquinones and 1,3-dicarbonyl compounds. | 2009 Oct 7 |
|
| Highly active gold-based catalyst for the reaction of benzaldehyde with ethyl diazoacetate. | 2009 Sep 14 |
|
| A short synthesis of the triazolopyrimidine antibiotic essramycin. | 2010 Nov 29 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:50:28 GMT 2023
by
admin
on
Fri Dec 15 16:50:28 GMT 2023
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| Record UNII |
K8CHJ4MKM0
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| Record Status |
Validated (UNII)
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| Record Version |
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JECFA EVALUATION |
ETHYL BENZOYLACETATE
Created by
admin on Fri Dec 15 16:50:28 GMT 2023 , Edited by admin on Fri Dec 15 16:50:28 GMT 2023
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CFR |
21 CFR 172.515
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admin on Fri Dec 15 16:50:28 GMT 2023 , Edited by admin on Fri Dec 15 16:50:28 GMT 2023
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202-295-3
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