444892-59-5 Usage
Uses
Used in Pharmaceutical Research:
T-BUTYL4-[2-AMINO-1-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]PIPERAZINE CARBOXYLATE is employed as a research chemical in the pharmaceutical industry for its potential role in drug development. Its unique structure allows it to be studied for interactions with biological targets, which could lead to the discovery of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, T-BUTYL4-[2-AMINO-1-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]PIPERAZINE CARBOXYLATE is used as a compound of interest for the design and synthesis of new pharmaceuticals. Its functional groups and structural elements can be modified to explore various chemical and biological properties, potentially leading to the creation of novel drugs with specific therapeutic effects.
Used in Drug Development:
T-BUTYL4-[2-AMINO-1-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]PIPERAZINE CARBOXYLATE is utilized in drug development as a starting material or a building block for the synthesis of new drug candidates. Its chemical properties and reactivity can be harnessed to create molecules with desired pharmacological profiles, targeting specific diseases or conditions.
Used in Chemical Synthesis:
In the broader chemical synthesis industry, T-BUTYL4-[2-AMINO-1-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]PIPERAZINE CARBOXYLATE may be used as an intermediate or a reactant in the synthesis of other complex organic compounds. Its versatility in chemical reactions can contribute to the production of specialty chemicals for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 444892-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,8,9 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 444892-59:
(8*4)+(7*4)+(6*4)+(5*8)+(4*9)+(3*2)+(2*5)+(1*9)=185
185 % 10 = 5
So 444892-59-5 is a valid CAS Registry Number.
444892-59-5Relevant academic research and scientific papers
Privileged structure based ligands for melanocortin receptors - Substituted benzylic piperazine derivatives
Fisher, Matthew J.,Backer, Ryan T.,Collado, Ivan,De Frutos, Oscar,Husain, Saba,Hsiung, Hansen M.,Kuklish, Steve L.,Mateo, Ana I.,Mullaney, Jeffrey T.,Ornstein, Paul L.,Paredes, Cristina Garcia,O'Brian, Thomas P.,Richardson, Timothy I.,Shah, Jikesh,Zgombick, John M.,Briner, Karin
, p. 4973 - 4978 (2007/10/03)
Replacement of the aryl piperazine moiety in compound 1 with a variety of substituted benzylic piperazines (6) yields compounds that afford melanocortin receptor 4 (MCR4) activity. Analogs with ortho substitution on the aromatic ring afforded the highest
