8-Chloro-2-methoxy-1,5-naphthyridine - 249889-68-7

8-Chloro-2-methoxy-1,5-naphthyridine

Catalog Number: EVT-3161935
CAS Number: 249889-68-7
Molecular Formula: C9H7ClN2O
Molecular Weight: 194.62 g/mol
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Product Introduction

Description
8-Chloro-2-methoxy-1,5-naphthyridine is a chemical compound that belongs to the naphthyridine family. It has gained significant attention in scientific research due to its potential biological activity and diverse applications. This paper aims to provide an overview of the synthesis methods, chemical structure, biological activity, biological effects, applications, and future perspectives of 8-Chloro-2-methoxy-1,5-naphthyridine.
Applications in Various Fields
In Medical Research, 8-Chloro-2-methoxy-1,5-naphthyridine has shown promise in drug development. It has been investigated as a potential candidate for the treatment of cancer, bacterial infections, and viral diseases. Clinical trials are underway to evaluate its efficacy and safety in humans. However, potential side effects and long-term effects need to be carefully monitored.
In Environmental Research, the compound's effects on ecosystems and its role in pollution management are being explored. Its potential impact on aquatic organisms and the environment requires thorough investigation to ensure sustainability and minimize adverse effects.
In Industrial Research, 8-Chloro-2-methoxy-1,5-naphthyridine finds applications in manufacturing processes. It can be used to improve product quality and efficiency in various industries. However, health and safety considerations must be taken into account to protect workers and prevent environmental contamination.

Properties

CAS Number

249889-68-7

Product Name

8-Chloro-2-methoxy-1,5-naphthyridine

IUPAC Name

8-chloro-2-methoxy-1,5-naphthyridine

Molecular Formula

C9H7ClN2O

Molecular Weight

194.62 g/mol

InChI

InChI=1S/C9H7ClN2O/c1-13-8-3-2-7-9(12-8)6(10)4-5-11-7/h2-5H,1H3

InChI Key

OPAVZRJSEDSFMQ-UHFFFAOYSA-N

SMILES

COC1=NC2=C(C=CN=C2C=C1)Cl

Canonical SMILES

COC1=NC2=C(C=CN=C2C=C1)Cl
Method of Synthesis or Extraction
Several methods have been developed for the synthesis of 8-Chloro-2-methoxy-1,5-naphthyridine. One commonly used method involves the reaction of 2-methoxy-1,5-naphthyridine with thionyl chloride and chloroform. This method offers a high yield and efficiency in the synthesis process. Another method involves the reaction of 2-methoxy-1,5-naphthyridine with chloroacetyl chloride and sodium hydroxide. This method also provides a good yield and is relatively simple to perform.
Environmental and safety considerations are crucial in the synthesis of 8-Chloro-2-methoxy-1,5-naphthyridine. Proper handling and disposal of chemicals, adherence to safety protocols, and waste management are essential to minimize environmental impact and ensure the safety of researchers.
Chemical Structure and Biological Activity
The chemical structure of 8-Chloro-2-methoxy-1,5-naphthyridine consists of a naphthyridine ring with a chlorine atom and a methoxy group attached at specific positions. This structure plays a vital role in its biological activity.
The compound exhibits potent biological activity due to its mechanism of action and interaction with biological targets. It has been found to inhibit the activity of certain enzymes involved in cell signaling pathways, leading to the modulation of various cellular processes. Additionally, 8-Chloro-2-methoxy-1,5-naphthyridine has shown promising activity against specific biological targets, such as cancer cells, bacteria, and viruses.
Biological Effects
The compound's effects on cell function and signal transduction are significant. It has been observed to interfere with key cellular processes, including cell proliferation, apoptosis, and DNA replication. By modulating these processes, 8-Chloro-2-methoxy-1,5-naphthyridine can potentially exert therapeutic effects in various diseases.
However, the compound's potent biological activity also raises concerns about potential toxic effects. Further studies are needed to evaluate its safety profile and determine the optimal dosage for therapeutic applications.
Future Perspectives and Challenges
Despite the promising potential of 8-Chloro-2-methoxy-1,5-naphthyridine, there are current limitations in its use and study. Further research is needed to fully understand its mechanism of action, optimize synthesis methods, and evaluate its long-term effects.
Possible solutions and improvements include the development of more efficient and environmentally friendly synthesis methods, as well as the identification of specific biological targets for therapeutic applications. Future trends and prospects in the application of 8-Chloro-2-methoxy-1,5-naphthyridine in scientific research include personalized medicine, targeted drug delivery, and combination therapies.
In conclusion, 8-Chloro-2-methoxy-1,5-naphthyridine holds great potential in various fields, including medical, environmental, and industrial research. Its synthesis methods, chemical structure, biological activity, and applications provide a foundation for further exploration and development. However, careful consideration of environmental and safety aspects, as well as addressing current limitations, is crucial for its successful utilization in scientific research.

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