88877-11-6 Usage
Chemical family
Naphthyridine derivatives This compound belongs to a group of chemical compounds that have a naphthyridine core structure.
Heterocyclic compound
Yes It is a compound with a ring structure containing both carbon and nitrogen atoms.
Core structure
1,6-Naphthyridine ring The central structure of the compound is a 1,6-naphthyridine ring, which is a seven-membered nitrogen-containing ring fused to a six-membered carbon ring.
Functional group
Carbonyl group The compound contains a carbonyl group (C=O) attached to the 2-position of the naphthyridine ring.
Substitution
Two methyl groups The compound has two methyl groups (CH3) attached at the 1 and 5 positions of the naphthyridine ring.
Potential applications
Medicinal chemistry and drug discovery Due to its unique structural features and potential biological activities, this compound may have applications in the development of new drugs and therapeutic agents.
Further research
Chemical properties and potential uses More research is needed to explore the compound's chemical properties, reactivity, and potential applications in various industrial and scientific fields.
Registry number
9CI The compound is registered with the CAS number 9CI, which is a unique identifier used in chemical databases and literature.
Molecular weight
Approximately 190 g/mol The molecular weight is an estimate of the mass of one mole of the compound, which can be calculated from its molecular formula.
Check Digit Verification of cas no
The CAS Registry Mumber 88877-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88877-11:
(7*8)+(6*8)+(5*8)+(4*7)+(3*7)+(2*1)+(1*1)=196
196 % 10 = 6
So 88877-11-6 is a valid CAS Registry Number.
88877-11-6Relevant articles and documents
A Facile and Novel Synthesis of 1,6-Naphthyridin-2(1H)-ones
Singh, Baldev,Lesher, George Y.
, p. 2085 - 2091 (2007/10/02)
A new and convenient procedure for the synthesis of 1,6-naphthyridin-2(1H)-ones and their derivatives is described.In the first scheme 5-acetyl-6--1,2-dihydro-2-oxo-3-pyridinecarbonitrile (4) obtained by the reaction of N,N-dimet
Certain 2-(1H)-pyridinones cardiotonic compositions containing same and method of using same
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, (2008/06/13)
1-R"-3-Q-4-R'-5-R-1,6-naphthyridin-2(1H)-ones (I) or salts thereof, where R is lower-alkyl, R' is hydrogen or methyl, R" is hydrogen or lower-alkyl, and Q is hydrogen, hydroxy, amino, cyano, carbamyl, carboxy or aminocarbamyl, are useful as cardiotonic ag
