115626-59-0 Usage
Description
(R)-Ethyl-2-hydroxypentanoate, with the molecular formula C7H14O3, is a colorless liquid characterized by a sweet, fruity odor. It is a chiral compound, featuring two enantiomers, (R)and (S)forms, with the (R)-form predominantly utilized in commercial applications. Derived from natural sources, it is deemed safe for use in the food and cosmetic industries, showcasing its versatility as a chemical compound with a spectrum of industrial and commercial applications.
Uses
Used in the Food Industry:
(R)-Ethyl-2-hydroxypentanoate is used as a flavoring agent for its sweet, fruity odor, enhancing the taste and aroma of various food products.
Used in the Perfume Industry:
It serves as a key component in the production of perfumes, capitalizing on its sweet, fruity scent to contribute to the overall fragrance profile of the product.
Used as a Solvent in Chemical Processes:
(R)-Ethyl-2-hydroxypentanoate is employed as a solvent in various chemical processes, leveraging its properties to facilitate reactions and improve efficiency in the production of different chemicals and compounds.
Used in the Cosmetic Industry:
It is utilized in the formulation of cosmetic products, taking advantage of its natural derivation and safety profile to ensure the well-being of consumers while also enhancing the product's sensory attributes.
Check Digit Verification of cas no
The CAS Registry Mumber 115626-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,2 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115626-59:
(8*1)+(7*1)+(6*5)+(5*6)+(4*2)+(3*6)+(2*5)+(1*9)=120
120 % 10 = 0
So 115626-59-0 is a valid CAS Registry Number.
115626-59-0Relevant articles and documents
Unusual Reduction of an α-Oxo Ester by Lithium Diisopropylamide
Hoare, John Harold,Yates, Peter
, p. 3333 - 3334 (1983)
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SARTAN ANALOGUE
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Page/Page column 9; 10; 18; 21; 22, (2019/07/23)
The invention concerns a sartan analogue on basis of a sartan which sartan comprises an alkyl group or an alkoxy group, wherein the sartan analogue only differs from the sartan by a replacement of the alkyl group or the alkoxy group or replacement of a methyl residue or a hydrogen residue of the alkyl group or of the alkoxy group by a fluorine atom.
Enantioselective catalytic synthesis of ethyl mandelate derivatives using Rh(I)-NHC catalysts and organoboron reagents
Marques, Carolina S.,Burke, Anthony J.
, p. 628 - 632 (2013/07/19)
Herein we describe for the first time the enantioselective catalytic arylation of ethyl glyoxalate using phenylboron reagents and chiral rhodium(I)-NHC catalysts. KOtBu was the base of choice, along with tert-amyl alcohol as the solvent. A novel chiral bis-imidazolium salt was synthesized and evaluated for the first time in this catalytic transformation. Although moderate enantioselectivities (up to 34% ee) were obtained for the phenylation reaction, despite the excellent yields, very low enantioselectivities were obtained using other arylboronic acids with a variety of chiral rhodium(I)-NHC catalysts.
