170164-47-3 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(S)-tert-Butyl 3-carbaMoylpiperazine-1-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals and bioactive compounds due to its unique chemical structure and reactivity. Its ability to form stable bonds with other molecules makes it a promising candidate for the development of new drugs with improved efficacy and safety profiles.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-tert-Butyl 3-carbaMoylpiperazine-1-carboxylate serves as a versatile building block for the creation of complex organic molecules. Its reactivity allows for the formation of various functional groups, enabling the synthesis of a wide range of compounds with diverse applications.
Used in Enzyme Inhibition Studies:
(S)-tert-Butyl 3-carbaMoylpiperazine-1-carboxylate has shown potential as an inhibitor for certain enzymes, making it a valuable tool in the study of enzyme function and the development of enzyme-targeted therapies. Its ability to modulate enzyme activity may contribute to the discovery of new treatments for various diseases and conditions.
Used in Medicinal Chemistry:
In medicinal chemistry, (S)-tert-Butyl 3-carbaMoylpiperazine-1-carboxylate is utilized for its potential therapeutic applications. Its pharmacological properties are being investigated to identify new drug targets and develop novel therapeutic agents with improved efficacy and reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 170164-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,1,6 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 170164-47:
(8*1)+(7*7)+(6*0)+(5*1)+(4*6)+(3*4)+(2*4)+(1*7)=113
113 % 10 = 3
So 170164-47-3 is a valid CAS Registry Number.
170164-47-3Relevant academic research and scientific papers
Kinetic resolution of piperazine-2-carboxamide by leucine aminopeptidase. An application in the synthesis of the nucleoside transport blocker (-)draflazine
Bruce,St. Laurent,Poindexter,Monkovic,Huang,Balasubramanian
, p. 2673 - 2684 (2007/10/02)
The resolution of N-t-Boc-piperazine carboxamide 5 proceeded smoothly in the presence of leucine aminopeptidase to produce acid (S)-1 and amide (R)-5 with good optical purity. Sequential alkylation and functional group manipulation of carboxamide (S)-5 provided the known nucleoside transport blocker (-)draflazine 2.
