170947-82-7 Usage
Description
(2S,4S)-1-BOC-4-BENZYLPYRROLIDINE-2-DICARBOXYLIC ACID ETHYL ESTER is a pyrrolidine derivative that serves as a chiral building block in organic synthesis and pharmaceutical research. (2S,4S)-1-BOC-4-BENZYLPYRROLIDINE-2-DICARBOXYLIC ACID ETHYL ESTER is distinguished by its BOC-protected amine group and a benzyl substituent on the pyrrolidine ring, along with being an ethyl ester of pyrrolidine-2,4-dicarboxylic acid, which endows it with enhanced reactivity and versatility in chemical reactions. Its unique structural features and chiral properties make it a promising candidate for the synthesis of pharmaceuticals and other biologically active compounds.
Uses
Used in Pharmaceutical Research:
(2S,4S)-1-BOC-4-BENZYLPYRROLIDINE-2-DICARBOXYLIC ACID ETHYL ESTER is used as a chiral building block for the development of pharmaceuticals, leveraging its unique stereochemistry to create enantiomerically pure compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (2S,4S)-1-BOC-4-BENZYLPYRROLIDINE-2-DICARBOXYLIC ACID ETHYL ESTER is utilized as a versatile intermediate, allowing for the creation of a wide range of chemical entities, including biologically active molecules, due to its reactivity and structural attributes.
Used in the Synthesis of Biologically Active Compounds:
(2S,4S)-1-BOC-4-BENZYLPYRROLIDINE-2-DICARBOXYLIC ACID ETHYL ESTER is employed as a key component in the synthesis of biologically active compounds, capitalizing on its structural features to produce molecules with potential applications in medicine and biology.
Check Digit Verification of cas no
The CAS Registry Mumber 170947-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,9,4 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 170947-82:
(8*1)+(7*7)+(6*0)+(5*9)+(4*4)+(3*7)+(2*8)+(1*2)=157
157 % 10 = 7
So 170947-82-7 is a valid CAS Registry Number.
170947-82-7Relevant articles and documents
New enantioselective approach to α-allokainoids by Michael addition to chiral 4-substituted 2,3-didehydroprolinate
Ezquerra,Ezquerra, Jesus,Escribano,Escribano, Ana,Rubio,Rubio, Almudena,Remuinan,Remuinan, Modesto Jesus,Vaquero,Josevaquero, Juan
, p. 6149 - 6152 (2007/10/02)
(-) and (+) α-Allokainoids hydrochlorides 3 and 4 were obtained by hydrolysis of the corresponding Michael adducts resulting from the addition of diethyl malonate to chiral N-urethane protected ethyl 4-benzyl-2,3-didehydroprolinates 9 and 13 respectively.
