5415-85-0 Usage
Description
Benzenepropanoic acid, .alpha.-phenyl-, ethyl ester is a chemical compound with the molecular formula C11H14O2. It is a colorless liquid characterized by a sweet, floral odor. This organic ester is known for its applications in various industries, including perfumery, flavoring, and pharmaceuticals.
Uses
Used in Perfumery and Fragrance Industry:
Benzenepropanoic acid, .alpha.-phenyl-, ethyl ester serves as a key ingredient in the production of perfumes and fragrances, where it is valued for its sweet, floral scent. It contributes to the creation of complex and pleasant aromas in a wide range of scented products.
Used in Food and Beverage Industry:
In the food and beverage sector, Benzenepropanoic acid, .alpha.-phenyl-, ethyl ester is utilized as a flavoring agent. Its distinctive sweet and floral notes enhance the taste and aroma of various food products and beverages, adding depth and complexity to their flavor profiles.
Used in Pharmaceutical Industry:
Benzenepropanoic acid, .alpha.-phenyl-, ethyl ester plays a crucial role in the pharmaceutical industry as an intermediate in the synthesis of different medications. Its chemical properties make it a versatile building block for developing new drugs and improving existing ones.
Safety Precautions:
It is essential to handle Benzenepropanoic acid, .alpha.-phenyl-, ethyl ester with care due to its potential to cause skin and eye irritation. Proper safety guidelines should be followed during its storage and handling to minimize risks and ensure the well-being of those who work with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 5415-85-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5415-85:
(6*5)+(5*4)+(4*1)+(3*5)+(2*8)+(1*5)=90
90 % 10 = 0
So 5415-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O2/c1-2-19-17(18)16(15-11-7-4-8-12-15)13-14-9-5-3-6-10-14/h3-12,16H,2,13H2,1H3
5415-85-0Relevant articles and documents
Cobalt-Catalyzed Aerobic Oxidative Cleavage of Alkyl Aldehydes: Synthesis of Ketones, Esters, Amides, and α-Ketoamides
Li, Tingting,Hammond, Gerald B.,Xu, Bo
supporting information, p. 9737 - 9741 (2021/05/31)
A widely applicable approach was developed to synthesize ketones, esters, amides via the oxidative C?C bond cleavage of readily available alkyl aldehydes. Green and abundant molecular oxygen (O2) was used as the oxidant, and base metals (cobalt and copper) were used as the catalysts. This strategy can be extended to the one-pot synthesis of ketones from primary alcohols and α-ketoamides from aldehydes.
Visible-light photocatalytic reduction of sulfonium salts as a source of aryl radicals
Donck, Simon,Baroudi, Abdulkader,Fensterbank, Louis,Goddard, Jean-Philippe,Ollivier, Cyril
, p. 1477 - 1482 (2013/06/27)
Triarylsulfonium salts are prompted to undergo efficient homolytic reduction by single electron transfer under mild photocatalytic conditions. The liberated aryl radical can then participate in carbon-carbon bond formation processes with allyl sulfones and activated olefins. Triarylsulfonium salts emerge as a valuable and alternative source of aryl radicals for synthesis. Copyright
Photochemical Reaction of Ethyl 3-Oxo-2,4-diphenylbutanoate
Yoshioka, Michikazu,Osawa, Haruhiko,Fukuzawa, Shinji
, p. 877 - 879 (2007/10/02)
Irradiation of ethyl 3-oxo-2,4-diphenylbutanoate in hexane gave the products formed by recombination of the radicals (Ph-CH2 and/or Ph-CH-CO2Et)resulting from decarbonylation, together with small amounts of 1,2-diphenylethanol and ethyl α-hydroxyphenylacetate, whereas in benzene no 1,2-diphenylethanol was found.Under oxygen an increased amount of ethyl α-hydroxyphenylacetate and no radical recombination products were observed.