93182-17-3 Usage
Chemical Structure
A complex structure consisting of a piperidine ring with a hydroxyl group attached to the fourth position, a pyridazine ring with a naphthalene group attached to the sixth position, and a 1-yl group attached to the third position.
Pharmaceutical Research Interest
Due to its potential biological activities, 1-(6-naphthalen-1-ylpyridazin-3-yl)piperidin-4-ol is of interest in pharmaceutical research.
Potential Applications
It may have implications in fields such as medicine, biochemistry, and neuroscience.
Development of New Drugs
It could potentially be used in the development of new drugs.
Research Tool
It could serve as a tool for studying biological processes.
Further Research Required
Its precise properties and potential applications would require further research and investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 93182-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,8 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93182-17:
(7*9)+(6*3)+(5*1)+(4*8)+(3*2)+(2*1)+(1*7)=133
133 % 10 = 3
So 93182-17-3 is a valid CAS Registry Number.
93182-17-3Relevant academic research and scientific papers
Synthesis and activity of 6-aryl-3-(hydroxypolymethyleneamino)pyridazines in animal models of epilepsy
Hallot,Brodin,Merlier,Brochard,Chambon,Biziere
, p. 369 - 375 (2007/10/02)
A series of 6-aryl-3-(hydroxypolymethyleneamino)pyridazines derivatives was synthesized and evaluated for anticonvulsant activity. The compounds were screened in mice for their ability to antagonize maximal electroshock- and bicuculline-induced seizures;
