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580-15-4

6-Aminoquinoline

Catalog#: AR0039BB  |   CAS#: 580-15-4  |   MDL#: MFCD00006803  |   MF: C9H8N2  |   MW: 144.1732

Packsize Purity Price Availability Quantity
1g 98% $3.00 Global Stock Buy Now Add To Cart
5g 98% $9.00 Global Stock Buy Now Add To Cart
10g 98% $15.00 Global Stock Buy Now Add To Cart
25g 98% $36.00 Global Stock Buy Now Add To Cart
100g 98% $125.00 Global Stock Buy Now Add To Cart
500g 98% $530.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0039BB
Chemical Name 6-Aminoquinoline
CAS Number 580-15-4
Molecular Formula C9H8N2
Molecular Weight 144.1732
MDL Number MFCD00006803
SMILES Nc1ccc2c(c1)cccn2
NSC Number 58388

6-Aminoquinoline is a versatile organic compound widely utilized in chemical synthesis as a key building block for various reactions and transformations. Its unique chemical structure and properties make it an invaluable reagent in the creation of numerous pharmaceuticals, agrochemicals, and fine chemicals.One prominent application of 6-Aminoquinoline is its role as a precursor in the synthesis of antimalarial drugs such as chloroquine and amodiaquine. By undergoing selective functional group modifications, 6-Aminoquinoline can be tailored to introduce specific pharmacophores crucial for the desired biological activity. This highlights its importance in the pharmaceutical industry for combating malaria, a widespread disease affecting millions of people globally.Additionally, 6-Aminoquinoline is utilized in the synthesis of fluorescent dyes and imaging agents due to its ability to form stable complexes with various metal ions. These metal complexes exhibit unique photophysical properties, making them valuable tools in biological imaging, sensor development, and molecular detection applications.Furthermore, 6-Aminoquinoline can serve as a key intermediate in the preparation of heterocyclic compounds, which are prevalent in medicinal chemistry and materials science. Its versatile reactivity allows for the construction of diverse molecular architectures through cyclization, substitution, and coupling reactions, enabling the synthesis of novel compounds with tailored properties and functions.Overall, the significance of 6-Aminoquinoline in chemical synthesis lies in its versatility, enabling the creation of a wide range of compounds essential for pharmaceuticals, materials, and biological research. Its strategic position as a key building block underscores its importance in advancing various fields of science and innovation.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H315-H319
Precautionary Statements P305+P351+P338
Class N/A
Packing Group N/A

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