2510-99-8

Basic information

• Product Name: ETHYL 2-PHENYLPROPIONATE
• Synonyms: RARECHEM AL BI 0123;ETHYL 2-PHENYLPROPIONATE;2-PHENYL PROPIONIC ACID ETHYL ESTER;alpha-methyl-benzeneaceticaciethylester;3-Ethyl-4-Methyl-2-Oxo-Pyrroline;ethyl hydratropate;Benzeneacetic acid, .alpha.-methyl-, ethyl ester;(2S)-2-Phenylpropionic acid ethyl ester
• CAS NO: 2510-99-8
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• EINECS: 219-727-1
• Product Categories: Benzene series;Aliphatics;Esters
• Mol File: 2510-99-8.mol
• Article Data: 93

Chemical Properties

• Boiling Point: 122°C 20mm
• Flash Point: 93.6 °C
• Appearance: /
• Density: 1.012 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Sparingly, Heated, Sonicated), Ethyl Acetate (Slightly)
• CAS DataBase Reference: ETHYL 2-PHENYLPROPIONATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-PHENYLPROPIONATE(2510-99-8)
• EPA Substance Registry System: ETHYL 2-PHENYLPROPIONATE(2510-99-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 2510-99-8(Hazardous Substances Data)

Usage

Chemical Properties

Colorless Liquid

Uses

2-Phenylpropionic Acid Ethyl Ester (cas# 2510-99-8) is a compound useful in organic synthesis.

InChI:InChI=1/C11H14O2/c1-3-13-11(12)9(2)10-7-5-4-6-8-10/h4-9H,3H2,1-2H3

Upstream product

• 64-17-5 ethanol 
• 492-37-5 hydratropic acid 
• 92582-40-6 (+/-)-2-Methyl-2-phenyl-3-oxo-bernsteinsaeure-diethylester 
• 101-97-3 Ethyl 2-phenylethanoate 
• 74-88-4 methyl iodide 
• 83-13-6 diethyl 2-phenylmalonate 
• 118778-90-8 5-Methyl-2-[1-methyl-2-oxo-2-phenyl-eth-(E)-ylidene]-5-phenyl-[1,3]dithiolan-4-one 
• 201230-82-2 carbon monoxide 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 15295-60-0 phenylpropionaldehyde diethyl acetal 
• 6084-17-9 2-chloro-1-phenylpropan-1-one 
• 122-51-0 orthoformic acid triethyl ester 
• 1823-91-2 1-phenylethyl cyanide 
• 1125-70-8 2-phenylpropanamide 

Downstream Products

• 14116-43-9 2-(4-methoxyphenyl)-6-phenyl-4H-pyran-4-one 
• 107451-78-5 5-(4-methoxyphenyl)-1-phenylpent-1-yne-3,5-dione 
• 4610-69-9 (Z)-ethyl cinnamate 
• 3677-70-1 1,1,2-triphenylprop-1-ene 
• 67631-84-9 N-(2-Benzylamino-ethyl)-2-phenyl-propionamide 
• 55453-62-8 2-[3-(6-Methoxy-benzofuran-2-carbonyl)-phenyl]-propionic acid 
• 55453-60-6 2-[3-(5-Methoxy-benzofuran-2-carbonyl)-phenyl]-propionic acid 
• 41387-29-5 2-[4-(acetyl)phenyl] propanoic acid 
• 95480-36-7 2-(3-acetylphenyl) propanoic acid 
• 53676-48-5 ethyl 2-(4-acetylphenyl)propanoate 
• 55453-46-8 ethyl 2-(3-acetylphenyl)propanoate 
• 55453-45-7 ethyl 2-[meta-(α-bromo-acetyl)phenyl]propionate 
• 105166-30-1 diethyl 2-methyl-2-phenylhexanedioate 
• 7782-24-3 (S)-2-Phenylpropionic acid 

Relevant articles and documents

Method for synthesizing P-bromomethyl isobenzopropionic acid

The invention provides a method for synthesizing p-bromomethyl isobenzopropionic acid, and relates to the technical field of organic synthesis. The synthesis method disclosed by the invention comprises the synthesis of isobenzoates. Vilsmeier Reagent preparation method comprises the following steps: synthesizing aldehyde isopropylparaben, synthesizing methyl isopropylbenzene, separating and purifying bromomethyl isobenzopropionic acid and, and the like. The final para-position selectivity of the method can reach 90 - 97%, and the three-waste yield is greatly reduced.

Photocatalytic acyl azolium-promoted alkoxycarbonylation of trifluoroborates

Despite recent advancements in the selective generation and coupling of organic radical species, the alkoxycarbonyl radical remains underexplored relative to other carbon-containing radical species. Drawing inspiration from new strategies for generating acyl radical equivalents utilizing dual N-heterocyclic carbene catalysis and photocatalysis, we have prepared dimethylimidazolium esters that can function as an alkoxycarbonyl radical surrogate under photocatalytic conditions. We demonstrate the synthetic utility of these azolium-based partners through the preparation of esters arising from the coupling of this radical surrogate with an oxidatively generated alkyl radical.