3-Boc-Amino-4-bromopyridine

95%

Reagent Code: #145641
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CAS Number 885275-14-9

science Other reagents with same CAS 885275-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.13 g/mol
Formula C₁₀H₁₃BrN₂O₂
thermostat Physical Properties
Melting Point 230-235°C
Boiling Point 391.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active pyridine derivatives. The Boc-protected amine allows for selective deprotection and further functionalization, while the bromine atom enables cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders. Its structure supports the construction of complex heterocyclic systems found in modern therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,090.00
inventory 1g
10-20 days ฿10,210.00

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3-Boc-Amino-4-bromopyridine
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active pyridine derivatives. The Boc-protected amine allows for selective deprotection and further functionalization, while the bromine atom enables cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders. Its structure supports the constr

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active pyridine derivatives. The Boc-protected amine allows for selective deprotection and further functionalization, while the bromine atom enables cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders. Its structure supports the construction of complex heterocyclic systems found in modern therapeutic agents.

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