1603-79-8
Chemical Structure
Ethyl phenylglyoxylate
Synonym(s): Ethyl benzoylformate; Phenylglyoxylic acid ethyl ester
- CAS No.: 1603-79-8
- Formula:C10H10O3
- Molecular Weight:178.19
IUPAC Name: Ethyl 2-oxo-2-phenylacetate
InChIKey: QKLCQKPAECHXCQ-UHFFFAOYSA-N
SMILES: CCOC(C(C1=CC=CC=C1)=O)=O
Biological Activity: Ethyl phenylglyoxylate (Ethyl benzoylformate), the ethyl ester of phenylglyoxylic acid, is used as a synthetic reagent. Ethyl phenylglyoxylate is also a poor substrate but a potent inhibitor of chicken liver carboxylesterase. Additionally, Ethyl phenylglyoxylate exhibits photoreactivity, where its excited triplet carbonyl can initiate intermolecular hydrogen abstraction, radical coupling and cross-linking reactions[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Ethyl phenylglyoxylate | 98.31% | Ethyl phenylglyoxylate (Ethyl benzoylformate), the ethyl ester of phenylglyoxylic acid, is used as a synthetic reagent. Ethyl phenylglyoxylate is also a poor substrate but a potent inhibitor of chicken liver carboxylesterase. Additionally, Ethyl phenylglyoxylate exhibits photoreactivity, where its excited triplet carbonyl can initiate intermolecular hydrogen abstraction, radical coupling and cross-linking reactions. | ||||||||||||||||||||
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Ethyl phenylglyoxylate (Standard) | 98.11% | Ethyl phenylglyoxylate (Ethyl benzoylformate) (Standard) is the analytical standard of Ethyl phenylglyoxylate (HY-W016618). This product is intended for research and analytical applications. Ethyl phenylglyoxylate (Ethyl benzoylformate), the ethyl ester of phenylglyoxylic acid, is used as a synthetic reagent. Ethyl phenylglyoxylate is also a poor substrate but a potent inhibitor of chicken liver carboxylesterase. Additionally, Ethyl phenylglyoxylate exhibits photoreactivity, where its excited triplet carbonyl can initiate intermolecular hydrogen abstraction, radical coupling and cross-linking reactions. | ||||||||||||||||||||
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Ethyl phenylglyoxylate-d5 | Ethyl phenylglyoxylate-d5 (Ethyl benzoylformate-d5; Phenylglyoxylic acid ethyl ester-d5) is the deuterium labeled Ethyl phenylglyoxylate (HY-W016618). Ethyl phenylglyoxylate (Ethyl benzoylformate), the ethyl ester of phenylglyoxylic acid, is used as a synthetic reagent. Ethyl phenylglyoxylate is also a poor substrate but a potent inhibitor of chicken liver carboxylesterase. Additionally, Ethyl phenylglyoxylate exhibits photoreactivity, where its excited triplet carbonyl can initiate intermolecular hydrogen abstraction, radical coupling and cross-linking reactions. | |||||||||||||||||||||
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Similarity Score 0.89
HY-W019643Glycopyrronium impurity 3 -
Similarity Score 0.86
HY-W017439Ethyl benzoate -
Similarity Score 0.85
HY-W010255APhenylglyoxylic acid sodium -
Similarity Score 0.83
HY-W018758R1-Phenylpropane-1,2-dione (Standard) -
Similarity Score 0.83
HY-W010255RPhenylglyoxylic acid (Standard) -
Similarity Score 0.83
HY-W750144Phenylglyoxylic acid-13C8 -
Similarity Score 0.82
HY-W027038Ethyl mandelate -
Similarity Score 0.82
HY-W099420RPropyl benzoate (Standard) -
Similarity Score 0.82
HY-W013607Benzoylacetone -
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References
- [1]. Shengkui Hu, et al. Photochemically Active Polymers Containing Pendant Ethyl Phenylglyoxylate. Macromolecules 1998, 31, 2, 322–327.
- [2]. Hu S, et al. Photoreduction of ethyl phenylglyoxylate. Journal of Photochemistry and Photobiology A: Chemistry, 1998, 114(2): 103-108.
- [3]. Berndt M C, et al. Ethyl phenylglyoxylate, a simultaneous inhibitor and substrate of chicken liver carboxylesterase (EC 3.1. 1.1). Enzyme-catalyzed fragmentation of (E)-benzil monoxime O-2, 4-dinitrophenyl ether. Journal of the American Chemical Society, 1977, 99(25): 8334-8335.
