90392-05-5 Usage
Uses
Used in Chemical Synthesis:
1,3-Dioxane-2-carboxylic acid, ethyl ester (9CI) is used as a solvent for facilitating various chemical reactions. Its ability to dissolve a wide range of substances makes it a valuable component in the synthesis of organic compounds.
Used in Flavor and Fragrance Industry:
1,3-Dioxane-2-carboxylic acid, ethyl ester (9CI) is used as a flavoring agent in food products, enhancing the taste and aroma of various culinary creations. Its unique properties allow it to contribute to the overall sensory experience of food items.
Used in Personal Care Products:
In the personal care industry, 1,3-Dioxane-2-carboxylic acid, ethyl ester (9CI) is used as a fragrance ingredient. Its incorporation into products such as perfumes, lotions, and shampoos helps to create appealing scents that are both long-lasting and pleasant.
However, it is crucial to handle 1,3-Dioxane-2-carboxylic acid, ethyl ester (9CI) with care due to potential health risks if not used properly. Proper safety measures and guidelines should be followed to ensure the safe use of this chemical in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90392-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,9 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90392-05:
(7*9)+(6*0)+(5*3)+(4*9)+(3*2)+(2*0)+(1*5)=125
125 % 10 = 5
So 90392-05-5 is a valid CAS Registry Number.
90392-05-5Relevant academic research and scientific papers
Direct anti-selective asymmetric hydrogenation of α-amino-β-keto esters through dynamic kinetic resolution using Ru-axially chiral phosphine catalysts-stereoselective synthesis of anti-β-hydroxy-α-amino acids
Makino, Kazuishi,Goto, Takayuki,Hiroki, Yasuhiro,Hamada, Yasumasa
experimental part, p. 2816 - 2828 (2009/06/28)
The asymmetric hydrogenation of α-amino-β-keto esters using ruthenium (Ru) anti-selectively proceeds via a dynamic kinetic resolution to afford anti-β-hydroxy-α-amino acids with high enantiomeric purities, which are important chiral building blocks for the synthesis of medicines and natural products. A mechanistic investigation has revealed that the Ru-catalyzed asymmetric hydrogenation takes place via the hydrogenation of the double bond in the enol tautomer of the substrate.
