78069-99-5 Usage
Uses
Used in Pharmaceutical Research:
1-(4-chlorophenyl)-2-methyl-4-(3-nitropyridin-4-yl)piperazine is used as a research compound for exploring its potential in medicinal chemistry. Its unique molecular structure may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-chlorophenyl)-2-methyl-4-(3-nitropyridin-4-yl)piperazine is used as a starting point for designing and synthesizing new drugs. Its complex structure and potential pharmacological properties make it a valuable tool for creating novel therapeutic agents.
Used in Drug Development:
1-(4-chlorophenyl)-2-methyl-4-(3-nitropyridin-4-yl)piperazine is utilized as a compound in the drug development process. Its properties may be harnessed to create drugs that can modulate specific biological pathways, potentially leading to treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 78069-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,6 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78069-99:
(7*7)+(6*8)+(5*0)+(4*6)+(3*9)+(2*9)+(1*9)=175
175 % 10 = 5
So 78069-99-5 is a valid CAS Registry Number.
78069-99-5Relevant academic research and scientific papers
Quantitative Structure Activity Relationship in 3,4-Disubstituted Pyridines and 1-(3"-Amino-4"-pyridyl)-4-arylpiperazines
Saxena, Anil K.,Arunamurthy, V.,Patnaik, G. K.,Jain, Padam C.,Anand, Nitya
, p. 873 - 878 (2007/10/02)
In a study of the SAR in 3,4-disubstituted pyridines, it has been observed that both stimulant and anticonvulsant activities are confined to 1-(3'-amino-4'-pyridyl)-4-phenylpiperazines, and further the substitution in the phenyl ring can dissociate these activities of this prototype.In order to understand the relationship of electronic (?), hydrophobic (?) and stereo (Es) parameters of the substituents with anticonvulsant activity, a multi-parameter regression analysis of twelve compounds of this group has been carried out, which suggests that hydrophobic and electronic factors are more important and anticonvulsant activity can be enhanced by compounds having log P = 2.7- 3.1 0= 2.67 (Eq. 5) and (log P)0= 3.09 (Eq. 6)> with an electron withdrawing substituent in the phenyl ring.
