≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ethyl benzoylacetate is an ester. It undergoes microbial reduction by bakers′ yeast (Saccharomyces cerevisiae), Beauveria sulfurescens or Geotrichum candidum to afford ethyl (S)-3-hydroxy-3-phenylpropionate.It undergoes Claisen condensation reaction with malononitrile to afford 2-cyano-5-phenyl-3,5-dioxopentanonitrile which on cyclization followed by coupling with diazonium salts yields azo derivatives.
Ethyl benzoylacetate (Benzoylacetic acid ethyl ester) was used to prepare ethyl 2-fluoro-2-benzolyacetate.It was also used to synthesize iodonium ylides.
| Pubchem Sid | 504751263 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751263 |
| Sourires canoniques | CCOC(=O)CC(=O)C1=CC=CC=C1 |
| IUPAC Name | ethyl 3-oxo-3-phenylpropanoate |
| 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 |
| Isomères SMILES | CCOC(=O)CC(=O)C1=CC=CC=C1 |
| WGK Allemagne | 2 |
| RTECS | AF4878000 |
| Poids moléculaire | 192.21 |
| Beilstein | 389944 |
| Reaxy-Rn | 389944 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=389944&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones - Aryl ketones - Phenylketones |
| Direct Parent | Alkyl-phenylketones |
| Alternative Parents | Benzoyl derivatives Aryl alkyl ketones Fatty acid esters Beta-keto acids and derivatives 1,3-dicarbonyl compounds Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Alkyl-phenylketone - Benzoyl - Aryl alkyl ketone - Beta-keto acid - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - 1,3-dicarbonyl compound - Keto acid - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 H2505099 | Certificate of Analysis | Aug 08, 2025 | E107010 |
| E2129145 | Certificate of Analysis | Mar 03, 2025 | E107010 |
| E2129147 | Certificate of Analysis | Mar 03, 2025 | E107010 |
| C2004096 | Certificate of Analysis | Dec 18, 2023 | E107010 |
| K1913077 | Certificate of Analysis | Sep 04, 2023 | E107010 |
| G2307743 | Certificate of Analysis | May 31, 2022 | E107010 |
| G2307745 | Certificate of Analysis | May 31, 2022 | E107010 |
| H2211050 | Certificate of Analysis | May 31, 2022 | E107010 |
| H2211133 | Certificate of Analysis | May 31, 2022 | E107010 |
| H2211134 | Certificate of Analysis | May 31, 2022 | E107010 |
| Solubilité | Miscible with ethanol and ether. Immiscible with water. |
|---|---|
| Sensibilité | Light & Air Sensitive |
| Indice de réfraction | 1.52 |
| Point d'éclair (°F) | 284 °F |
| Point d'éclair (°C) | 140℃ |
| Point d'ébullition (°C) | 265-270°C |
| Poids moléculaire | 192.210 g/mol |
| XLogP3 | 1.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 192.079 Da |
| Monoisotopic Mass | 192.079 Da |
| Topological Polar Surface Area | 43.400 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 205.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Junyi Tang, Yuanyuan Ren, Jiachun Feng. (2022) Fluorescence-color-changing biomimetic tough films with simultaneous shape-deformation triggered by pH. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2022.135932] |
| 2. Zixu Zhang, Zikun Wang, Hongliang Mu, Xin Wang, Yunhui Li, Jingling Yan, Zhen Wang. (2017) A novel approach to 1,2,3-triazole grafted chitosans via modified Wolff’s cyclocondensation. EUROPEAN POLYMER JOURNAL, [PMID:] [10.1016/j.eurpolymj.2017.11.047] |
| 3. Xinyue Guo, Qiyue Zhou, Xuefeng Fan, Qinyan Zhu, Ming Jin. (2024) Heteroatom/Heterocycle-Substituted Ketone Dyes as Efficient Photoinitiators in Visible Light-Emitting Diode/Near Infrared Light Photopolymerization with Enhanced Two-Photon Lithography Capability. ACS Applied Polymer Materials, [PMID:] [10.1021/acsapm.4c00932] |
