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PHENYL ETHYL PROPIONATE FOR SYNTHESIS PRODUCT CODE CASR NO. 188745 SYNONYMS Phenethyl propionate C.I. NO. -- (122-70-3) ATOMIC ORMOLECULAR FORMULA OC 11 H 14 2 ATOMIC ORMOLECULAR WEIGHT 178.23 PROPERTIES -- C 11 H 14 O 2 PARAMETER LIMIT Description Colourless liquid. Solubility Miscible with alcohols and ether. Minimum assay (GC) 0 98.0%.The invention relates to the technical field of chemical synthesis, and particularly relates to a preparation method for synthesis of ethyl 3-ethoxypropionate; the ethyl 3-ethoxypropionate is synthesized by addition reaction of absolute ethanol and ethyl acrylate in the presence of a catalyst in a tubular reactor, the molar ratio of absolute ethanol to ethyl acrylate is 3: 1 to 100: 1, the.Ethyl propionate is a propanoate ester of ethanol. It has a role as a metabolite. Ethyl propionate appears as a clear colorless liquid with a pineapple-like odor.
The invention belongs to the technical field of chemical synthesis, and in particular relates to a method for preparing 3-ethoxy ethyl propionate. The method comprises a synthesizing step and a refining step, wherein the synthesizing step adopts ethanol and ethyl acrylate as raw materials to carry out addition under the action of a catalyst, and the catalyst adopts alkali metal or alkali.
Reference(s) for synthesis of 2-Phenylethyl propionate Al Neirabeyeh, M., and Pujol, M.D. 1990. New oxidative esterification of alcohols with aldehydes by the Br2-HMPT-NaHCO3.
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One hundred and thirty-eight grams (175 cc., 3 moles) of absolute ethyl alcohol is added drop by drop through the funnel (Note 1). After the alcohol has been added and there is no unchanged sodium (as evidenced by cessation of boiling) the flask is immersed in an ice-water bath, and a mixture of 306 g. (3 moles) of ethyl propionate and 438 g.
In this microscale chemistry experiment, from the Royal Society of Chemistry, benzoic acid is warmed with ethanol in a plastic pipette, the ester ethylbenzoate, is identified by smell. The resource is set out as teachers' notes followed by the students' page which presents the task to be investigated. A list of apparatus and chemicals needed for the investigation is provided, together with.
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This substance is used in the following activities or processes at workplace: transfer of chemicals, roller or brushing applications, non-industrial spraying, closed, continuous processes with occasional controlled exposure, closed processes with no likelihood of exposure, batch processing in synthesis or formulation with opportunity for exposure and treatment of articles by dipping and pouring.
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CAS: 105-37-3 MDL: MFCD00009308 EINECS: 203-291-4 Synonyms: Propionic acid ethyl ester.
Methyl propiolate was used in the synthesis of polysubstituted 3-arylaminoacrylate and tetrahydropyrimidin-2-one derivatives. It was also used as a thiol derivatizing agent for capillary electrophoresis.
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Effect of Solvents and Kinetic Parameters on Synthesis of Ethyl Propionate Catalysed by Poly (AAc-co-HPMA-cl-MBAm)-Matrix-Immobilized Lipase of Pseudomonas aeruginosa BTS-2.
Methyl and ethyl esters are commonly available for many amino acids; the t -butyl ester tends to be more expensive. However, t -butyl esters are particularly useful because, under strongly acidic conditions, the t -butyl esters undergo elimination to give the carboxylic acid and isobutylene, simplifying work-up.
BUTYL PROPIONATE 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.