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3-(4-Methoxyphenyl)-6-(4-morpholinyl)pyridazino(4,3-c)isoquinoline is a complex organic compound with a molecular formula of C26H23N3O2. It is characterized by a pyridazinone core, which is fused with an isoquinoline ring. The compound features a 4-methoxyphenyl group attached at the 3-position and a 4-morpholinyl group at the 6-position. This specific arrangement of functional groups gives the molecule unique chemical and biological properties. It is often studied for its potential applications in medicinal chemistry, particularly in the development of new drugs targeting various biological pathways. The compound's structure allows for interactions with specific receptors or enzymes, which can lead to therapeutic effects. Its synthesis and biological evaluation are of interest to researchers in the field of drug discovery and development.

96825-92-2

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96825-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96825-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,2 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96825-92:
(7*9)+(6*6)+(5*8)+(4*2)+(3*5)+(2*9)+(1*2)=182
182 % 10 = 2
So 96825-92-2 is a valid CAS Registry Number.

96825-92-2Downstream Products

96825-92-2Relevant academic research and scientific papers

Pyridazino[4,3-c]-isoquinolines having anti-anxiety activity

-

, (2008/06/13)

The present invention is directed to pyridazino[4,3-c]isoquinolines of Formula I STR1 wherein R represents methyl, phenyl or substituted phenyl groups, R 1 represents inter alia amino or substituted amino, alkoxy or cycloalkoxy groups, having pharmacologi

Benzodiazepine receptor binding and anticonflict activity in a series of 3,6-disubstituted pyridazino[4,3-c]isoquinolines devoid of anticonvulsant properties

Toja,Tarzia,Barone,Luzzani,Gallico

, p. 1314 - 1319 (2007/10/02)

A series of 3,6-disubstituted pyridazino [4,3-c]isoquinolines were synthesized and tested for their ability to inhibit the binding of [3H]diazepam to rat brain receptors in vitro. Compounds bearing a phenyl, 4-methyoxyphenyl, or methyl group at

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