77762-97-1 Usage
Molecular structure
2,6-bis[4-(piperidin-1-yl)but-2-yn-1-yl]pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone consists of a pyrrolo[3,4-f]isoindole core with two piperidine and two but-2-yn-1-yl groups attached.
Type of compound
It is a tetrone compound, which means it contains four carbonyl groups (C=O) within its structure.
Functional groups
The presence of multiple functional groups, such as piperidine, but-2-yn-1-yl, and carbonyl groups, contribute to its high functionalization and potential reactivity.
Potential applications
Due to its complex structure and multiple functional groups, this compound has potential applications in medicinal chemistry (e.g., drug development) and material science (e.g., synthesis of new materials with unique properties or activities).
Need for further research
To fully understand the potential uses and properties of 2,6-bis[4-(piperidin-1-yl)but-2-yn-1-yl]pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetrone, additional research and testing are necessary. This includes studying its chemical reactivity, stability, and potential interactions with biological systems or other materials.
Check Digit Verification of cas no
The CAS Registry Mumber 77762-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,6 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77762-97:
(7*7)+(6*7)+(5*7)+(4*6)+(3*2)+(2*9)+(1*7)=181
181 % 10 = 1
So 77762-97-1 is a valid CAS Registry Number.
77762-97-1Relevant articles and documents
Synthesis and biological evaluation of N,N'-di-(4-t-amino-2-butynyl) pyromellitic acid diimides
Eldeen,Cosmo,Ghantous,Khayat
, p. 91 - 93 (2007/10/02)
A series of N,N'-di-(4-t-amino-2-butynyl) pyomellitic acid diimides have been prepared and investigated for blocking of the motor effects of oxotreorine in intact mice and for their antagonistic activity towards acetylcholine on isolated guinea-pig ileal preparations. None of the prepared derivatives showed oxotremorine antagonistic activity but all have an acetylcholine antagonistic activity except the one in which the cyclic amine is piperidine.
