tert-Butyl (4-(aminomethyl)pyridin-2-yl)carbamate

95%

Reagent Code: #144252
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CAS Number 639091-78-4

science Other reagents with same CAS 639091-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.27 g/mol
Formula C₁₁H₁₇N₃O₂
badge Registry Numbers
MDL Number MFCD06213871
thermostat Physical Properties
Melting Point 131-132 °C
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

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 allows for selective modification in drug design, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in the preparation of protease inhibitors and receptor antagonists due to the protected amine group, which enables controlled deprotection and coupling in multi-step reactions. Also utilized in the production of agrochemicals and specialty chemicals requiring stable amine functionalities.

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Test Parameter Specification
Purity (HPLC) 94.5-100
Infrared Spectrum Conforms to Structure
Appearance yellow-orange powder

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,990.00
inventory 1g
10-20 days ฿9,960.00

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tert-Butyl (4-(aminomethyl)pyridin-2-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 biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in the preparation of protease inhibitors and receptor antagonists due to the protected amine group, which enables controlled deprotection and coupling in multi-step reactions. Also utiliz

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in the preparation of protease inhibitors and receptor antagonists due to the protected amine group, which enables controlled deprotection and coupling in multi-step reactions. Also utilized in the production of agrochemicals and specialty chemicals requiring stable amine functionalities.

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