87850-83-7 Usage
Description
Ethyl 3-(6-oxopiperidin-3-yl)propanoate is a chemical compound with the molecular formula C11H17NO3. It is a propanoic acid derivative with a piperidin-3-one moiety, and it is classified as an ester. ethyl 3-(6-oxopiperidin-3-yl)propanoate can be synthesized through the reaction of ethyl acetoacetate with piperidine-3-one in the presence of a base.
Uses
Used in Pharmaceutical Industry:
Ethyl 3-(6-oxopiperidin-3-yl)propanoate is used as an intermediate in organic synthesis for the preparation of pharmaceuticals. Its unique structure allows it to be a key component in the development of various drug molecules.
Used in Agrochemical Industry:
Ethyl 3-(6-oxopiperidin-3-yl)propanoate is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Material Development:
ethyl 3-(6-oxopiperidin-3-yl)propanoate has potential applications in the development of new materials, where its specific chemical properties can be utilized to create innovative and improved materials for various industries.
Used in Chemical Research:
Ethyl 3-(6-oxopiperidin-3-yl)propanoate is utilized in chemical research to explore its properties and potential reactions, further expanding the understanding of its applications and possibilities in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 87850-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,5 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87850-83:
(7*8)+(6*7)+(5*8)+(4*5)+(3*0)+(2*8)+(1*3)=177
177 % 10 = 7
So 87850-83-7 is a valid CAS Registry Number.
87850-83-7Relevant articles and documents
Enamines and iminium salts from amino-acids
McHintosh, John M.,Pillon, Lilianna Z.,Acquaah, Samuel O.,Green, James R.,White, Graham S.
, p. 2016 - 2021 (2007/10/02)
Distillation of ω-carboxyalkyl lactams from soda-lime leads to the formation of bicyclic enamines or imines with concomitant loss of carbon dioxide and water.Monoamides of dicarboxylic acids afford cyclic ketones.A mechanistic rationale is presented and it is concluded that the reaction is a variant of the classical Ruzicka cyclization of dicarboxylic acids.The method allows the regiospecific formation of iminium salts of bicyclic nitrogen heterocycles.
