110545-79-4 Usage
Molecular structure
The compound has a complex molecular structure that includes a benzene ring and a naphthyridine ring.
3-chlorophenyl group
The presence of a 3-chlorophenyl group in its structure denotes a chlorine atom attached to a phenyl group, which may confer specific chemical properties to the compound.
Tetrahydrobenzo[b][1,8]naphthyridin-5(7H)-one backbone
The compound has a tetrahydrobenzo[b][1,8]naphthyridin-5(7H)-one backbone, which is likely to have pharmacological relevance.
Potential applications
The compound may serve as a scaffold for drug development or as a biological probe in research.
Contribution to medicinal chemistry
Further study and characterization of this compound could contribute to the advancement of medicinal chemistry and pharmaceutical innovation.
Chemical properties
The compound may exhibit specific chemical properties due to the presence of the 3-chlorophenyl group.
Biological activity
The compound may have potential biological activity due to its complex molecular structure and pharmacological relevance.
Synthesis
The compound may be synthesized through various chemical reactions and techniques.
Stability
The compound may have specific stability properties depending on its molecular structure and functional groups.
Solubility
The compound's solubility properties may be influenced by its molecular structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 110545-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,4 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110545-79:
(8*1)+(7*1)+(6*0)+(5*5)+(4*4)+(3*5)+(2*7)+(1*9)=94
94 % 10 = 4
So 110545-79-4 is a valid CAS Registry Number.
110545-79-4Relevant articles and documents
Intramolecular transaminations of enaminones: A synthesis of fused, polycyclic, N-aryl pyridones
Friary,Seidl,Schwerdt,Cohen,Hou,Nafissi
, p. 7169 - 7178 (1993)
2-Arylamino-3-pyridinecarbonyl chlorides acylated the β-carbon atoms of enamines, and the resulting enaminones cyclized to give a series of fused polycyclic N-aryl pyridones. The series included 10-(3-chlorophenyl)-6,8,9,10-tetrahydrobenzo[b][1,8]naphthyr
Synthesis and characterisation of medium-sized ring systems by oxidative cleavage. Part 2: Insights from the study of ring expanded analogues
Lebl, Tomas,Lorion, Magali M.,Jones, Alan M.,Philp, Douglas,Westwood, Nicholas J.
experimental part, p. 9694 - 9702 (2011/02/23)
Variable temperature NMR analysis and computational methods have been used to develop a detailed understanding of the 1H NMR spectra of a family of medium-sized ring containing compounds. The family consists of analogues containing 10-, 11- and
Polycyclic quinoline, naphthyridine and pyrazinopyridine derivatives
-
, (2008/06/13)
Novel polycyclic quinoline, naphthyridine and pyrazinopyridine derivatives are disclosed which are useful for treating allergic reactions, inflammation, peptic ulcers, hypertension, and hyperproliferative skin diseases and for suppressing the immune respo
