- Ethyl 3-phenylpropionate
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- $100.00 / 1KG
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2024-12-24
- CAS:2021-28-5
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| Ethyl 3-phenylpropionate Basic information |
| Ethyl 3-phenylpropionate Chemical Properties |
Melting point | 122-124 °C | Boiling point | 247-248 °C(lit.) | density | 1.01 g/mL at 25 °C(lit.) | refractive index | n20/D 1.494(lit.) | FEMA | | Fp | 226 °F | storage temp. | 2-8°C | solubility | Chloroform (Soluble), DMSO (Slightly), Methanol | form | Oil | color | Colourless | Specific Gravity | 1.013 | Odor | at 100.00 %. hyacinth rose honey fruity rum | Odor Type | floral | Water Solubility | <0.1 g/100 mL at 25 ºC | JECFA Number | 644 | BRN | 1910432 | InChIKey | JAGZUIGGHGTFHO-UHFFFAOYSA-N | LogP | 2.79 | CAS DataBase Reference | 2021-28-5(CAS DataBase Reference) | NIST Chemistry Reference | | EPA Substance Registry System | |
Safety Statements | 23-24/25 | WGK Germany | 3 | TSCA | Yes | HS Code | 29163900 |
| Ethyl 3-phenylpropionate Usage And Synthesis |
Chemical Properties | clear colorless to light yellow liquid | Chemical Properties | Ethyl 3-phenylpropionate has an ethereal, rum, fruity, floral odor. | Occurrence | Reported found in rum, passion fruit, plum brandy, caja fruit (Spondias lutea L.) and checkur (Alpinia sessilis). | Uses | Ethyl 3-phenylpropionate is used as an active pharmaceutical ingredient intermediate. It is also used in the synthesis of pyrimidine based inhibitors of cyclin-dependant kinases. | Preparation | By hydrogenation of the corresponding ethyl cinnamate in the presence of nickel in alcohol solution. | Definition | ChEBI: Ethyl 3-phenylpropanoate is a fatty acid ester. | Aroma threshold values | Detection: 17 to 40 ppb | Synthesis Reference(s) | The Journal of Organic Chemistry, 50, p. 3406, 1985 DOI: Synthetic Communications, 22, p. 2683, 1992 DOI: Tetrahedron Letters, 42, p. 781, 2001 DOI: | General Description | Clear colorless liquid. | Air & Water Reactions | Insoluble in water. | Reactivity Profile | Ethyl 3-phenylpropionate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. | Fire Hazard | The flash point of Ethyl 3-phenylpropionate has not been determined. but Ethyl 3-phenylpropionate is probably combustible. |
| Ethyl 3-phenylpropionate Preparation Products And Raw materials |
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