73193-59-6 Usage
Uses
Used in Pharmaceutical Industry:
Diethyl 3-oxopiperidine-1,4-dicarboxylate is used as a key intermediate in the synthesis of various drugs for its role in creating sedative or analgesic properties.
Used in Research and Development:
Diethyl 3-oxopiperidine-1,4-dicarboxylate is used as a research compound for medicinal and biochemical purposes, aiding in the advancement of pharmaceutical formulations and understanding of related chemical reactions.
Used in Production of Pharmaceuticals:
Diethyl 3-oxopiperidine-1,4-dicarboxylate is used as a component in the manufacturing process of pharmaceuticals, contributing to the development of new medications with potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 73193-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73193-59:
(7*7)+(6*3)+(5*1)+(4*9)+(3*3)+(2*5)+(1*9)=136
136 % 10 = 6
So 73193-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO5/c1-3-16-10(14)8-5-6-12(7-9(8)13)11(15)17-4-2/h8H,3-7H2,1-2H3
73193-59-6Relevant academic research and scientific papers
Specific Enolates from α-Amino Ketones
Garst, Michael E.,Bonfiglio, John N.,Grudoski, David A.,Marks, Jeffrey
, p. 2307 - 2315 (2007/10/02)
The enolization of 11 tertiary α-amino ketones was investigated under three different conditions (kinetic base, thermodynamic base, thermodynamic acid) to determine the directionality of such enolates for application to alkaloid synthesis.The ketone structural variables examined were the geometry of the amine nitrogen lone pair-carbonyl array and the electronic nature of the nitrogen substituent.With the exception of 3-pyrrolidinones, increasing the electron-withdrawing nature of the nitrogen increases the amount of enolization toward nitrogen (3, 6, and 9 or 21, 24, and 27).N-Alkyl-substituted amino ketones (3, 12, 21, 33) under kinetic base conditions yield enolate distributions similar to those of the corresponding all-carbon compounds.N-Carbamato-substituted amino ketones (6, 24, 27, 30) enolize predominantly toward nitrogen under all conditions.The 3-pyrrolidinones 12, 15, and 18 afford enolates away from nitrogen under all conditions.
