(2-aMino-pyridin-4-ylMethyl)-carbaMic acid tert-butyl ester

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Reagent Code: #203048
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CAS Number 474809-21-7

science Other reagents with same CAS 474809-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.2716 g/mol
Formula C₁₁H₁₇N₃O₂
badge Registry Numbers
MDL Number MFCD09028166
thermostat Physical Properties
Boiling Point 407.1±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.138±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl carbamate (Boc) protecting group allows for controlled amine reactivity during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like assembly processes. Commonly employed in medicinal chemistry for optimizing lead compounds in treatments targeting inflammatory diseases, cancer, and central nervous system disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,870.00
inventory 500mg
10-20 days ฿5,550.00
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(2-aMino-pyridin-4-ylMethyl)-carbaMic acid tert-butyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl carbamate (Boc) protecting group allows for controlled amine reactivity during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like assembly processes. Commonly employed in medicinal ch

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl carbamate (Boc) protecting group allows for controlled amine reactivity during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like assembly processes. Commonly employed in medicinal chemistry for optimizing lead compounds in treatments targeting inflammatory diseases, cancer, and central nervous system disorders.

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