886779-61-9 Usage
Uses
Used in Pharmaceutical Industry:
Tert-Butyl 3-tert-butylpiperazine-1-carboxylate hydrochloride is used as a key intermediate in the synthesis of medications for the treatment of schizophrenia and anxiety disorders. Its chemical structure allows for the development of drugs that can effectively address these conditions by modulating neurotransmitter levels and receptor interactions in the brain.
Used in Organic Synthesis:
In addition to its pharmaceutical applications, Tert-Butyl 3-tert-butylpiperazine-1-carboxylate hydrochloride can also be utilized in the synthesis of other organic compounds. Its unique structure and reactivity make it a valuable building block for the creation of various chemical entities, contributing to the advancement of chemical research and development.
Used in Chemical Research and Development:
Tert-Butyl 3-tert-butylpiperazine-1-carboxylate hydrochloride holds potential for further exploration in chemical research and development. Its properties and reactivity may lead to the discovery of new applications and uses in various fields, expanding its impact beyond the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 886779-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,7,7 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 886779-61:
(8*8)+(7*8)+(6*6)+(5*7)+(4*7)+(3*9)+(2*6)+(1*1)=259
259 % 10 = 9
So 886779-61-9 is a valid CAS Registry Number.
886779-61-9Relevant academic research and scientific papers
SnAP reagents for the synthesis of piperazines and morpholines
Luescher, Michael U.,Vo, Cam-Van T.,Bode, Jeffrey W.
, p. 1236 - 1239 (2014/03/21)
Substituted piperazines and morpholines are valuable structural motifs in biologically active compounds, but are not easily prepared by contemporary cross-coupling approaches. In this report, we introduce SnAP reagents for the transformation of aldehydes into N-unprotected piperazines and morpholines. This approach offers simple, mild conditions compatible with aromatic, heteroaromatic, aliphatic, and glyoxylic aldehydes and provides mono- and disubstituted N-heterocycles in a single step.
