54369-24-3 Usage
Uses
Used in Food and Beverage Industry:
Diethyl 2,3-diethyl-2-butenedioate is used as a flavoring agent for adding a sweet, fruity taste to various products. Its fruity odor and taste enhance the overall flavor profile of food and beverages, making them more appealing to consumers.
Used in Pharmaceutical and Organic Compound Synthesis:
Diethyl 2,3-diethyl-2-butenedioate is utilized as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure allows it to participate in a wide range of chemical reactions, making it a valuable building block in the development of new drugs and other chemical products.
Safety:
Diethyl 2,3-diethyl-2-butenedioate is considered to be relatively safe for use in food and other applications. However, it should still be handled with care and in accordance with proper safety guidelines to minimize any potential risks or adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 54369-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,6 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54369-24:
(7*5)+(6*4)+(5*3)+(4*6)+(3*9)+(2*2)+(1*4)=133
133 % 10 = 3
So 54369-24-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O4/c1-5-9(11(13)15-7-3)10(6-2)12(14)16-8-4/h5-8H2,1-4H3/b10-9+
54369-24-3Relevant academic research and scientific papers
Metallo-beta-lactamase inhibitors
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Page/Page column 18, (2010/11/30)
A new metallo-β-lactamase inhibitor which acts as a medicament for inhibiting the inactivation of β-lactam antibiotics and recovering anti-bacterial activities is disclosed. The maleic acid derivatives having the general formula (I) have metallo-β-lactamase inhibiting activities. It is possible to recover the anti-bacterial activities of β-lactam antibiotics against metallo-β-lactamase producing bacteria by combining the compound of the general formula (I) with β-lactam antibiotics.
DIALKYL-SUBSTITUTED MALEATES FROM α-BROMOESTERS
Hagiwara, H.,Sugioka, T.,Uda, H.
, p. 1193 - 1198 (2007/10/02)
Dialkyl-substituted maleates were prepared by the dimerization of α-bromoesters by treating with LDA and CuI.
