1-Boc-3-Bromo-7-nitroindole

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Reagent Code: #146155
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CAS Number 914349-37-4

science Other reagents with same CAS 914349-37-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.16 g/mol
Formula C₁₃H₁₃BrN₂O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The Boc-protected indole scaffold allows selective functionalization at specific positions, making it valuable in drug discovery. The bromo group enables cross-coupling reactions such as Suzuki or Heck reactions to introduce aromatic or alkenyl substituents. The nitro group can be reduced to an amine, enabling further derivatization for building complex heterocyclic systems. Commonly applied in the development of kinase inhibitors, antiviral agents, and other therapeutic targets involving indole-based structures. Its protected form enhances stability and solubility during multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿168.00
inventory 250mg
10-20 days ฿340.00
inventory 1g
10-20 days ฿780.00
inventory 5g
10-20 days ฿2,256.00

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1-Boc-3-Bromo-7-nitroindole
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. The Boc-protected indole scaffold allows selective functionalization at specific positions, making it valuable in drug discovery. The bromo group enables cross-coupling reactions such as Suzuki or Heck reactions to introduce aromatic or alkenyl substituents. The nitro group can be reduced to an amine, enabling further derivatization for building complex heterocyclic systems. Commonly applied in the development of kinase inhibitors, antiviral agents, and other therapeutic targets involving indole-based structures. Its protected form enhances stability and solubility during multi-step syntheses.
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