5174-94-7 Usage
Explanation
Different sources of media describe the Explanation of 5174-94-7 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 16 carbon (C) atoms, 11 hydrogen (H) atoms, and 3 nitrogen (N) atoms.
2. Organic compounds are chemical compounds that contain carbon and hydrogen atoms. This compound falls under this category as it contains both carbon and hydrogen atoms.
3. Aminopyridines are a subclass of organic compounds that consist of a pyridine ring with an amino group (-NH2) attached. This compound is a derivative of pyridine with an amino group at position 2.
4. The compound has an amino group (-NH2) at position 2 and a phenyl group (C6H5) at position 3 of the pyridine ring, which makes it a derivative of pyridine.
5. Due to its versatile reactivity and biological activity, this compound is commonly used in the synthesis of pharmaceutical drugs and agrochemicals.
6. The compound has potential applications in medicinal chemistry and drug discovery due to its ability to act as a building block for the synthesis of new compounds with therapeutic properties.
7. The compound has a fused structure consisting of a six-membered pyridine ring and a five-membered nitrogen-containing heterocycle (1,8-naphthyridine).
Class
Organic compounds
Subclass
Aminopyridines
Substitution
2-amino and 3-phenyl groups
Applications
Pharmaceutical drugs and agrochemicals
Potential Applications
Medicinal chemistry and drug discovery
Structure
Fused six-membered and five-membered nitrogen-containing heterocycles
Check Digit Verification of cas no
The CAS Registry Mumber 5174-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5174-94:
(6*5)+(5*1)+(4*7)+(3*4)+(2*9)+(1*4)=97
97 % 10 = 7
So 5174-94-7 is a valid CAS Registry Number.
5174-94-7Relevant articles and documents
Asymmetric P^N^P type ligand based on 2-aminotetrahydronaphthyridine as well as preparation method of ligand
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Paragraph 0038; 0039; 0060; 0061; 0071; 0072, (2019/02/27)
The invention belongs to the technical field of organic synthesis and discloses an asymmetric P^N^P type ligand based on 2-aminotetrahydronaphthyridine as well as a preparation method of the ligand. The ligand has the structure shown in a formula (I). The
Green Synthesis of Fused Imidazo[1,2-a][1,8]naphthyridine Derivatives Catalyzed by DABCO under Solvent-Free Solid-State Conditions and Their Biological Evaluation
Banoth, Sonyanaik,Perugu, Shyam,Boda, Sakram
, p. 709 - 715 (2018/01/22)
An efficient and eco-friendly methodology has been developed for the construction of fused imidazo[1,2-a][1,8]naphthyridine derivatives in the presence of 1,4-diazabicyclo[2.2.2]octane, and involving various substituted heterocyclic amines with phenacyl b
An Efficient Microwave-Assisted Synthesis of Novel 2-{4-[(3-Aryl-1,8-naphthyridin-2-yl)amino]phenyl}-1H-benzo[de]isoquinoline-1,3(2H)-diones and Their Antimicrobial Activity
Sakram,Ravi,Ashok,Rambabu,Sonyanaik,Kurumanna
, p. 780 - 788 (2018/06/14)
The Buchwald–Hartwig amination reaction between 2-chloro-3-aryl-1,8-naphthyridines and 2-(4-aminophenyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione in the presence of the catalytic system Pd(PPh3)4 and the base KO-t-Bu in toluene was studied. The reaction was initiated by microwave irradiation. Highly efficient synthesis has been developed for 2-{4-[(3-aryl-1,8-naphthyridin-2-yl)amino]phenyl}-1H-benzo[de]isoquinoline-1,3(2H)-diones. Structures of the synthesized compounds were evaluated by IR, 1H and 13C NMR spectroscopy. All products were tested for antimicrobial activity against Escheria coli, Bacillus subtilis, Klebsiella pneumoniae, and Staphylococcus aureus.
