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2-oxopropyl phenylacetate, also known as phenylacetic acid propionyl ester, is an organic compound with the chemical formula C11H12O3. It is a colorless to pale yellow liquid with a fruity, floral, and slightly spicy odor. This ester is formed by the reaction of phenylacetic acid and propionyl chloride, and it is widely used in the fragrance and flavor industry due to its pleasant aroma. It can be found in various applications, such as perfumes, cosmetics, and food products, where it imparts a sweet, fruity, and balsamic scent. Additionally, 2-oxopropyl phenylacetate has potential applications in the pharmaceutical industry as a chemical intermediate for the synthesis of various drugs.

5215-63-4

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5215-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5215-63-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5215-63:
(6*5)+(5*2)+(4*1)+(3*5)+(2*6)+(1*3)=74
74 % 10 = 4
So 5215-63-4 is a valid CAS Registry Number.

5215-63-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxopropyl 2-phenylacetate

1.2 Other means of identification

Product number -
Other names 2-oxopropyl phenylacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5215-63-4 SDS

5215-63-4Relevant academic research and scientific papers

Microwave-Enhanced Coupling of Carboxylic Acids with Liquid Ketones and Cyclic Ethers Using Tetrabutylammonium Iodide/ t-Butyl Hydroperoxide

Macías-Benítez, Pablo,Moreno-Dorado, F. Javier,Guerra, Francisco M.

, p. 6027 - 6043 (2020/05/22)

The oxidative coupling of carboxylic acids with liquid ketones and cyclic ethers has been accomplished in minutes using t-butyl hydroperoxide in the presence of tetrabutylammonium iodide under microwave irradiation in the absence of a solvent. In addition to drastically shortening the reaction times, the use of microwaves resulted, in general, in yields equal to or higher than those obtained by conventional heating.

Rearrangement of 2-bromo-1-(bromomethyl)ethyl esters under basic conditions: Scope and mechanism

Alliot, Julien,Gravel, Edmond,Doris, Eric

, p. 2861 - 2866 (2013/10/22)

A novel rearrangement of 2-bromo-1-(bromomethyl)ethyl esters into the corresponding 2-oxopropyl derivatives is reported. The mechanism of this transformation was studied by means of 18O- and 2H- labeling experiments. The reaction pro

Polymer supported reagents: Facile synthesis of β-oxalkyl (acetonyl) esters of carboxylic acids

Salunkhe, Manikrao M.,Sande, Amirhamja R.,Kanade, Annappa S.,Wadgaonkar, Prakash P.

, p. 2885 - 2891 (2007/10/03)

β-Oxoalkyl (acetonyl) esters have been synthesised in high yields and in a state of purity by reaction of chloroacetone with insoluble polymer supported carboxylate ions at room temperature.

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