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Home  > Chemistry  > Heterocyclic Building Blocks  > Naphthyridines  > 6-Chloro-2,7-naphthyridin-1(2H)-one

AA34780

1260663-93-1 | 6-Chloro-2,7-naphthyridin-1(2H)-one

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $13.00 $10.00 -   +
250mg 98% in stock $25.00 $18.00 -   +
500mg 98% in stock $49.00 $35.00 -   +
1g 98% in stock $73.00 $52.00 -   +
5g 98% in stock $364.00 $255.00 -   +
10g 98% in stock $727.00 $509.00 -   +
25g 98% in stock $1,572.00 $1,101.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA34780
Chemical Name: 6-Chloro-2,7-naphthyridin-1(2H)-one
CAS Number: 1260663-93-1
Molecular Formula: C8H5ClN2O
Molecular Weight: 180.5911
MDL Number: MFCD18250873
SMILES: Clc1ncc2c(c1)cc[nH]c2=O

 

Computed Properties
Complexity: 229  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • 6-Chloro-2,7-naphthyridin-1(2H)-one, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis processes. Its unique structure and reactive properties make it a valuable building block for the creation of various organic compounds.One key application of $name$ in chemical synthesis is as a precursor in the production of pharmaceutical intermediates. Due to its structural characteristics, $name$ can undergo various chemical transformations to introduce specific functional groups or modify existing ones, facilitating the synthesis of target molecules with potential pharmaceutical activity. By incorporating 6-Chloro-2,7-naphthyridin-1(2H)-one into synthetic routes, chemists can access a diverse range of pharmacologically relevant compounds for drug discovery and development.Moreover, $name$ can also serve as a key reagent in the construction of heterocyclic compounds. Its chloro-substituted naphthyridine scaffold can participate in a variety of cyclization reactions, enabling the formation of complex ring systems found in many natural products and biologically active molecules. This versatility makes 6-Chloro-2,7-naphthyridin-1(2H)-one a valuable tool for designing and synthesizing novel compounds with potential applications in medicinal chemistry, agrochemicals, and materials science.
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