(4-Methoxy-pyridin-2-yl)-carbamic acid tert-butyl ester

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Reagent Code: #129400
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CAS Number 551950-46-0

science Other reagents with same CAS 551950-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.26 g/mol
Formula C₁₁H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD05663515
thermostat Physical Properties
Melting Point 124-127 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocyclic compounds, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the amine during multi-step syntheses, allowing selective reactivity. The methoxy-pyridine moiety enhances solubility and can influence binding affinity to target proteins. Commonly employed in medicinal chemistry for lead optimization and library synthesis in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,370.00
inventory 1g
10-20 days ฿16,430.00

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(4-Methoxy-pyridin-2-yl)-carbamic acid tert-butyl ester
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocyclic compounds, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the amine during multi-step syntheses, allowing selective reactivity. The methoxy-pyridine moiety enhances solubility a

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocyclic compounds, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The tert-butyl carbamate (Boc) group provides protection for the amine during multi-step syntheses, allowing selective reactivity. The methoxy-pyridine moiety enhances solubility and can influence binding affinity to target proteins. Commonly employed in medicinal chemistry for lead optimization and library synthesis in drug discovery programs.

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