62295-41-4 Usage
Molecular structure
2-1-[2-(pyrrolidin-1-yl)ethyl]pyridin-4(1H)-ylidene-1H-indene-1,3(2H)-dione is a complex organic compound consisting of a pyrrolidine ring, a pyridine ring, and an indene-1,3-dione moiety.
Functional groups
The compound contains multiple functional groups, including a pyrrolidine ring, a pyridine ring, and an indene-1,3-dione moiety, which contribute to its potential biological or pharmacological activity.
Biological interaction
The presence of the pyrrolidine and pyridine rings may allow the compound to interact with biological targets, such as proteins or enzymes, potentially leading to pharmacological effects.
Structural diversity
The indene-1,3-dione moiety provides structural diversity to the compound, which may be important for its ability to bind to various biological targets and exhibit different activities.
Potential reactivity
The indene-1,3-dione moiety may also impart potential reactivity to the compound, allowing it to undergo chemical reactions or participate in biological processes.
Further analysis needed
To fully understand the chemical and biological properties of 2-1-[2-(pyrrolidin-1-yl)ethyl]pyridin-4(1H)-ylidene-1H-indene-1,3(2H)-dione, further analysis and characterization are necessary, such as determining its solubility, stability, and bioavailability.
Check Digit Verification of cas no
The CAS Registry Mumber 62295-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,9 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62295-41:
(7*6)+(6*2)+(5*2)+(4*9)+(3*5)+(2*4)+(1*1)=124
124 % 10 = 4
So 62295-41-4 is a valid CAS Registry Number.
62295-41-4Relevant articles and documents
Pyrophthalones. VI. 2-(N-alkyl-1,4-dihydropyridinyliden-4-yl)-1,3-indanediones. Research of antitumor activity
Letourneux,Sparfel,Roussakis,et al.
, p. 535 - 540 (2007/10/02)
N-alkylated derivatives of 2-(4-piridinyl)-1,3-indandiones have synthesized for the purpose of obtaining agents with tumor-inhibitory activity. Neither the introduction of an ω-amino group nor the presence of a chloro atom led to activity against L-1210 l
