886767-93-7 Usage
Uses
Used in Pharmaceutical Research and Development:
4-Boc-2-(4-(trifluoroMethyl)phenyl)piperazine is utilized as a key building block in the synthesis of pharmaceuticals and other biologically active molecules. Its distinctive structure allows for the creation of new compounds with potential therapeutic applications, making it an essential component in drug discovery and development.
Used in Chemical Synthesis:
In the chemical synthesis industry, 4-Boc-2-(4-(trifluoroMethyl)phenyl)piperazine is employed as a versatile intermediate for the production of various organic compounds. Its reactivity and functional groups enable it to participate in a range of chemical reactions, facilitating the synthesis of complex molecules with specific properties and applications.
It is crucial to handle and store 4-Boc-2-(4-(trifluoroMethyl)phenyl)piperazine with care due to its potential hazards, ensuring safety in research and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 886767-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,7,6 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 886767-93:
(8*8)+(7*8)+(6*6)+(5*7)+(4*6)+(3*7)+(2*9)+(1*3)=257
257 % 10 = 7
So 886767-93-7 is a valid CAS Registry Number.
886767-93-7Relevant articles and documents
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.
