Bi-Tert-Butyl (5-Bromopyridin-2-Yl)Carbamate

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Reagent Code: #151039
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CAS Number 209959-28-4

science Other reagents with same CAS 209959-28-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.24 g/mol
Formula C₁₅H₂₁BrN₂O₄
badge Registry Numbers
MDL Number MFCD18249958
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. The bromine substituent enables further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings for designing drug candidates targeting neurological disorders and cancer.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,070.00
inventory 1g
10-20 days ฿13,910.00
inventory 100mg
10-20 days ฿2,960.00

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Bi-Tert-Butyl (5-Bromopyridin-2-Yl)Carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. The bromine substituent enables further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings for de

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its protected amine functionality allows for selective reactions in multi-step organic syntheses. The bromine substituent enables further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings for designing drug candidates targeting neurological disorders and cancer.

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