tert-Butyl 4-((6-bromopyridin-2-yl)amino)piperidine-1-carboxylate

≥95%

Reagent Code: #149724
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CAS Number 1042224-77-0

science Other reagents with same CAS 1042224-77-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.26 g/mol
Formula C₁₅H₂₂BrN₃O₂
thermostat Physical Properties
Boiling Point 456.4±45.0℃(Predicted)
inventory_2 Storage & Handling
Storage 2-8℃, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in constructing bioactive molecules that modulate enzyme activity. Commonly employed in medicinal chemistry for building blocks in drug discovery programs, especially those focused on oncology and inflammatory diseases. The compound’s protected amine group facilitates stepwise synthesis, enabling efficient coupling and deprotection strategies in complex molecule assembly.

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inventory 1g
10-20 days ฿36,910.00

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tert-Butyl 4-((6-bromopyridin-2-yl)amino)piperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in constructing bioactive molecules that modulate enzyme activity. Commonly employed in medicinal chemistry for building blocks in drug discovery programs, especially those focused on oncology and inflammatory diseases. The compound’s protected amine group facilitates stepwise synthesis

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure allows for selective modification, making it valuable in constructing bioactive molecules that modulate enzyme activity. Commonly employed in medicinal chemistry for building blocks in drug discovery programs, especially those focused on oncology and inflammatory diseases. The compound’s protected amine group facilitates stepwise synthesis, enabling efficient coupling and deprotection strategies in complex molecule assembly.

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