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2-(4-Propyl-phenyl)-propionic acid ethyl ester is an organic compound with the chemical formula C14H20O2. It is an ester derivative of 2-(4-propyl-phenyl)-propionic acid, where the carboxylic acid group is esterified with ethanol. 2-(4-Propyl-phenyl)-propionic acid ethyl ester is characterized by a phenyl ring with a propyl group attached to the para position and a propionic acid chain with an additional propyl group. It is a colorless liquid with a fruity, floral odor and is commonly used in the fragrance industry as a fixative and in the flavor industry for its sweet, fruity taste. The compound is also known for its potential applications in the pharmaceutical and chemical industries.

3585-62-4

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3585-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3585-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3585-62:
(6*3)+(5*5)+(4*8)+(3*5)+(2*6)+(1*2)=104
104 % 10 = 4
So 3585-62-4 is a valid CAS Registry Number.

3585-62-4Upstream product

3585-62-4Relevant academic research and scientific papers

Synthesis method of carbonyl alpha-position monomethyl substituted compound

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Paragraph 0026-0029; 0039-0042; 0053-0057, (2022/01/12)

The invention discloses a synthesis method of a carbonyl alpha-position monomethyl substituted compound, thesynthesis method comprises the following steps: taking substituted phenylboronic acid and ethyl 2-bromoacrylate as raw materials, taking THF and water as solvents, reacting K2CO3 and a catalyst Pd (OAc) 2 under the protection of nitrogen, purifying to obtain an intermediate product, dissolving the intermediate product in a methanol solvent, performing catalytic hydrogenation, reacting at room temperature, filtering, and spin-drying the solvent to obtain the carbonyl alpha-position monomethyl substituted compound. According to the synthesis method of the carbonyl alpha-position monomethyl substituted compound, the target compound can be conveniently obtained, the toxicity of reagents participating in the reaction is small, and the reaction conditions are mild. Post-treatment is simple and safe, the product quality is good, and the method is suitable for large-scale production.

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