103-25-3
103-25-3
Chemical Structure
Methyl 3-phenylpropanoate
- CAS No.: 103-25-3
- Formula:C10H12O2
- Molecular Weight:164.20
IUPAC Name: methyl 3-phenylpropanoate
InChIKey: RPUSRLKKXPQSGP-UHFFFAOYSA-N
SMILES: O=C(OC)CCC1=CC=CC=C1
Biological Activity: Methyl 3-phenylpropanoate is a phenylpropionate compound. Methyl 3-phenylpropanoate derivatives interfere with insect feeding behavior. Methyl 3-phenylpropanoate can be used to study insect feeding behavior[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Methyl 3-phenylpropanoate | 99.88% | Methyl 3-phenylpropanoate is a phenylpropionate compound. Methyl 3-phenylpropanoate derivatives interfere with insect feeding behavior. Methyl 3-phenylpropanoate can be used to study insect feeding behavior. | ||||||||||||||||||||
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Methyl 3-phenylpropanoate (Standard) | ≥98% | Methyl 3-phenylpropanoate (Standard) is the analytical standard of Methyl 3-phenylpropanoate (HY-W007828). This product is intended for research and analytical applications. Methyl 3-phenylpropanoate is a phenylpropionate compound. Methyl 3-phenylpropanoate derivatives interfere with insect feeding behavior. Methyl 3-phenylpropanoate can be used to study insect feeding behavior. | ||||||||||||||||||||
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References
- [1]. Ernawati T, et al. Anti-inflammatory Activities of Methyl trans-Cinnamate derivatives on Carrageenan-Induced Paw Edema in Male Sprague Dawley Rats. Proceeding ISETH (International Summit on Science, Technology, and Humanity), 2019: 557-563.
- [2]. Bohman B, et al. Structure-activity relationships of phenylpropanoids as antifeedants for the pine weevil Hylobius abietis. J Chem Ecol. 2008 Mar;34(3):339-52. [Content Brief]
- [3]. Lu X, et al. Process Development of the Sharpless Catalytic Asymmetric Dihydroxylation Reaction To Prepare Methyl (2 R, 3 S)-2, 3-Dihydroxy-3-phenylpropionate. Organic Process Research & Development, 2000, 4(6): 575-576.
- [4]. Sasaki K, et al. C= C Double Bond Insertion in Catalytic C–H Activation. Dehydrogenative Cross Coupling of Arenes with Olefins. Chemistry Letters, 1988, 17(4): 685-688.
