62295-43-6 Usage
Molecular structure
Contains a piperidine ring, a pyridine ring, and an indene-1,3-dione moiety.
Segment attachment
Features a piperidine-ethyl-pyridine segment connected to an indene-1,3-dione group.
Biological properties
Likely to exhibit biological properties or pharmaceutical relevance due to the presence of multiple functional groups.
Aromatic characteristics
May possess aromatic properties, as it has a fused ring system with delocalized electrons.
Heterocyclic nature
The presence of multiple heteroatoms (e.g., nitrogen) in its structure contributes to its heterocyclic characteristics.
Chemical activities
The presence of various functional groups and heteroatoms may lead to different chemical activities and reactivities.
Further research
Additional research and analysis are required to fully understand the properties and potential applications of this complex organic compound.
Check Digit Verification of cas no
The CAS Registry Mumber 62295-43-6 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 62295-43:
(7*6)+(6*2)+(5*2)+(4*9)+(3*5)+(2*4)+(1*3)=126
126 % 10 = 6
So 62295-43-6 is a valid CAS Registry Number.
62295-43-6Relevant 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
