872973-92-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements, in this case, carbon, hydrogen, chlorine, nitrogen, and oxygen.
Explanation
The naphthyridine ring is a six-membered nitrogen-containing aromatic ring that is part of the compound's structure.
Explanation
The compound's structure and properties make it a candidate for use in the development of new pharmaceuticals.
Explanation
The dichlorophenyl group in the molecule may contribute to its biological activity, making it a potential candidate for use in the development of pesticides or herbicides.
Explanation
Further research is being conducted to explore the compound's properties, potential uses, and effects on various biological systems.
Explanation
This is the specific chemical structure and naming of the compound, which describes the arrangement of atoms and functional groups within the molecule.
Heterocyclic Compound
Yes
Naphtyridine Ring
Present
Chlorine Substituents
Attached to the phenyl ring
Potential Applications
Pharmaceutical industry, synthesis of novel drugs
Biological Activity
Potential use as a pesticide or herbicide
Ongoing Research
Properties and applications
Chemical Structure
1,6-Naphthyridin-2(1H)-one, 5,7-dichloro-1-(2,6-dichlorophenyl)-
Check Digit Verification of cas no
The CAS Registry Mumber 872973-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,9,7 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 872973-92:
(8*8)+(7*7)+(6*2)+(5*9)+(4*7)+(3*3)+(2*9)+(1*2)=227
227 % 10 = 7
So 872973-92-7 is a valid CAS Registry Number.
872973-92-7Relevant academic research and scientific papers
Efficient synthesis of a trisubstituted 1,6-naphthyridone from acetonedicarboxylate and regioselective Suzuki arylation
Chung, John Y. L.,Cai, Chaoxian,McWilliams, J. Christopher,Reamer, Robert A.,Dormer, Peter G.,Cvetovich, Raymond J.
, p. 10342 - 10347 (2007/10/03)
An efficient five-step synthesis of 1,6-naphthyridone 3b, a p38 mitogen-activated protein (MAP) kinase inhibitor intermediate, in 32% overall yield starting from acetonedicarboxylate (ADC) is described. The synthesis began with a selective monoamidation o
