3-Amino-4-(benzylamino)pyridine

Reagent Code: #44621
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CAS Number 57806-32-3

science Other reagents with same CAS 57806-32-3

blur_circular Chemical Specifications

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Weight 199.25 g/mol
Formula C₁₂H₁₃N₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique structure, featuring both amino and benzylamino groups, makes it valuable in the synthesis of pharmaceutical compounds, particularly those targeting neurological disorders. It is also employed in the creation of dyes and pigments, where its aromatic and amino functionalities contribute to the color properties and stability of the final product. Additionally, it finds use in research settings for the study of chemical reactions involving nitrogen-containing heterocycles, aiding in the development of new synthetic methodologies.

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inventory 200mg
10-20 days ฿9,000.00

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3-Amino-4-(benzylamino)pyridine
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This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique structure, featuring both amino and benzylamino groups, makes it valuable in the synthesis of pharmaceutical compounds, particularly those targeting neurological disorders. It is also employed in the creation of dyes and pigments, where its aromatic and amino functionalities contribute to the color properties and stability of the final product. Ad

This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical structures. Its unique structure, featuring both amino and benzylamino groups, makes it valuable in the synthesis of pharmaceutical compounds, particularly those targeting neurological disorders. It is also employed in the creation of dyes and pigments, where its aromatic and amino functionalities contribute to the color properties and stability of the final product. Additionally, it finds use in research settings for the study of chemical reactions involving nitrogen-containing heterocycles, aiding in the development of new synthetic methodologies.

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