tert-Butyl (3-formylpyridin-4-yl)carbamate

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Reagent Code: #145345
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CAS Number 116026-93-8

science Other reagents with same CAS 116026-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.24 g/mol
Formula C₁₁H₁₄N₂O₃
thermostat Physical Properties
Boiling Point 310°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. The aldehyde group allows for further functionalization via reactions such as reductive amination or Wittig reactions, enabling the construction of complex molecular structures. The tert-butyloxycarbonyl (Boc) protecting group stabilizes the amine during synthetic transformations and can be easily removed under mild acidic conditions when needed. Its structure is especially valuable in medicinal chemistry for designing drug candidates targeting neurological disorders and cancer.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,520.00
inventory 1g
10-20 days ฿4,800.00
inventory 5g
10-20 days ฿16,000.00
inventory 25g
10-20 days ฿56,000.00

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tert-Butyl (3-formylpyridin-4-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. The aldehyde group allows for further functionalization via reactions such as reductive amination or Wittig reactions, enabling the construction of complex molecular structures. The tert-butyloxycarbonyl (Boc) protecting group stabilizes the amine during synthetic transformations and can be easily removed under mild acidic conditions when needed. Its st

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. The aldehyde group allows for further functionalization via reactions such as reductive amination or Wittig reactions, enabling the construction of complex molecular structures. The tert-butyloxycarbonyl (Boc) protecting group stabilizes the amine during synthetic transformations and can be easily removed under mild acidic conditions when needed. Its structure is especially valuable in medicinal chemistry for designing drug candidates targeting neurological disorders and cancer.

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