tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate

95%

Reagent Code: #131386
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CAS Number 379264-77-4

science Other reagents with same CAS 379264-77-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.28 g/mol
Formula C₁₂H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD24476455
thermostat Physical Properties
Boiling Point 379.7±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.092±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used in pharmaceutical synthesis as a protected amine intermediate, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions to reveal the free amine for further coupling. The pyridin-4-yloxy moiety enhances binding affinity in receptor-targeted compounds, making this building block valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of cardiovascular agents, anti-inflammatory drugs, and central nervous system therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,420.00
inventory 250mg
10-20 days ฿24,620.00

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tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate
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Used in pharmaceutical synthesis as a protected amine intermediate, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions to reveal the free amine for further coupling. The pyridin-4-yloxy moiety enhances binding affinity in receptor-targeted compounds, making this building block valuable in medicinal chemistry for optimizing drug candidates. Common

Used in pharmaceutical synthesis as a protected amine intermediate, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides stability during reactions and can be easily removed under mild acidic conditions to reveal the free amine for further coupling. The pyridin-4-yloxy moiety enhances binding affinity in receptor-targeted compounds, making this building block valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of cardiovascular agents, anti-inflammatory drugs, and central nervous system therapeutics.

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