(2-Aminopyridin-3-yl)(phenyl)methanone

95%

Reagent Code: #36371
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CAS Number 3810-10-4

science Other reagents with same CAS 3810-10-4

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Weight 198.2206 g/mol
Formula C₁₂H₁₀N₂O
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MDL Number MFCD02258896
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(2-Aminopyridin-3-yl)(phenyl)methanone is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of heterocyclic molecules. Its structure, featuring both an aminopyridine and a phenyl group, makes it valuable for constructing complex molecules with potential therapeutic applications. This compound is often employed in the design of drug candidates targeting specific enzymes or receptors, particularly in the development of kinase inhibitors, which are important in cancer therapy. Additionally, it is used in the preparation of ligands for metal coordination chemistry, aiding in the study of catalytic processes and material science. Its versatility in chemical reactions, such as condensation and cyclization, makes it a valuable building block in medicinal chemistry and drug discovery.

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inventory 100mg
10-20 days ฿4,572.00

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(2-Aminopyridin-3-yl)(phenyl)methanone
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(2-Aminopyridin-3-yl)(phenyl)methanone is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of heterocyclic molecules. Its structure, featuring both an aminopyridine and a phenyl group, makes it valuable for constructing complex molecules with potential therapeutic applications. This compound is often employed in the design of drug candidates targeting specific enzymes or receptors, particularly in the development of kinase inhibitors, which are important in cancer therapy. Additionally, it is used in the preparation of ligands for metal coordination chemistry, aiding in the study of catalytic processes and material science. Its versatility in chemical reactions, such as condensation and cyclization, makes it a valuable building block in medicinal chemistry and drug discovery.
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