796856-41-2 Usage
Description
1-(2,6-dichloropyridin-4-yl)piperazine is a chemical compound with the molecular formula C9H11Cl2N3, belonging to the class of piperazine derivatives. It features a dichloropyridinyl group attached to the piperazine structure, which contributes to its diverse range of potential applications in the pharmaceutical industry.
Uses
Used in Pharmaceutical Research and Development:
1-(2,6-dichloropyridin-4-yl)piperazine is used as a building block for the synthesis of various biologically active molecules. Its unique chemical structure allows for the creation of new compounds with potential therapeutic benefits.
Used in the Development of Antipsychotic and Anxiolytic Agents:
1-(2,6-dichloropyridin-4-yl)piperazine is used as a precursor in the development of antipsychotic and anxiolytic agents. Its potential in this application has shown promising results in preclinical studies, indicating its value in the treatment of mental health disorders.
Used in Antimicrobial Applications:
1-(2,6-dichloropyridin-4-yl)piperazine is also being investigated for its potential antimicrobial properties. Its ability to inhibit the growth of harmful microorganisms could make it a valuable addition to the arsenal of antibiotics and antifungal agents.
Used in Anticancer Applications:
Furthermore, 1-(2,6-dichloropyridin-4-yl)piperazine has been explored for its potential anticancer properties. Its ability to target and disrupt cancer cell processes may contribute to the development of novel cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 796856-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,8,5 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 796856-41:
(8*7)+(7*9)+(6*6)+(5*8)+(4*5)+(3*6)+(2*4)+(1*1)=242
242 % 10 = 2
So 796856-41-2 is a valid CAS Registry Number.
796856-41-2Relevant articles and documents
First selective lithiation of pyridylpiperazines: Straightforward access to potent pharmacophores
Lou?rat, Frédéric,Gros, Philippe,Fort, Yves
, p. 4761 - 4768 (2007/10/03)
The three isomers of pyridylpiperazines have been lithiated for the first time. The use of a superbase, an aminoalkoxide containing lithiating agent overcomes the chelating influence of the basic piperazine nitrogens, so that selective mono lithiation occurred alpha to pyridine nitrogen. This methodology offers a new access to diverse potent pharmacophores not easily prepared by other routes.
