5-(Boc-amino)-2-(Boc-aminomethyl)pyridine

≥95%

Reagent Code: #69292
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CAS Number 1456821-59-2

science Other reagents with same CAS 1456821-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.39 g/mol
Formula C₁₆H₂₅N₃O₄
badge Registry Numbers
MDL Number MFCD26404527
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of active pharmaceutical ingredients (APIs) and other biologically active molecules. The Boc (tert-butoxycarbonyl) protecting groups in the compound are crucial for safeguarding the amine functionalities during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. It is often employed in peptide synthesis, where controlled deprotection of the Boc groups allows for the sequential assembly of peptide chains. Additionally, it finds application in the development of small molecule inhibitors and other therapeutic agents, particularly in the fields of oncology and neurology, where precise chemical modifications are essential for optimizing drug efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,830.00
inventory 1g
10-20 days ฿41,805.00
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5-(Boc-amino)-2-(Boc-aminomethyl)pyridine
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This chemical is primarily used in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of active pharmaceutical ingredients (APIs) and other biologically active molecules. The Boc (tert-butoxycarbonyl) protecting groups in the compound are crucial for safeguarding the amine functionalities during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. It is ofte

This chemical is primarily used in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the preparation of active pharmaceutical ingredients (APIs) and other biologically active molecules. The Boc (tert-butoxycarbonyl) protecting groups in the compound are crucial for safeguarding the amine functionalities during multi-step synthetic processes, ensuring selective reactions and preventing unwanted side reactions. It is often employed in peptide synthesis, where controlled deprotection of the Boc groups allows for the sequential assembly of peptide chains. Additionally, it finds application in the development of small molecule inhibitors and other therapeutic agents, particularly in the fields of oncology and neurology, where precise chemical modifications are essential for optimizing drug efficacy and selectivity.

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