tert-Butyl (4-chloropyridin-2-yl)carbamate

98%

Reagent Code: #145160
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CAS Number 130721-78-7

science Other reagents with same CAS 130721-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.68 g/mol
Formula C₁₀H₁₃ClN₂O₂
thermostat Physical Properties
Boiling Point 274.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It serves as a protected amine building block in medicinal chemistry, enabling selective reactions at other functional sites during multi-step syntheses. Commonly employed in the preparation of bioactive molecules targeting inflammatory and oncological pathways. Its stability under various reaction conditions makes it valuable in solid-phase and solution-phase peptide-like synthesis. Also utilized in agrochemical research for constructing nitrogen-containing heterocycles with pesticidal activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿960.00
inventory 10g
10-20 days ฿5,670.00
inventory 25g
10-20 days ฿14,150.00
inventory 100g
10-20 days ฿56,520.00
inventory 5g
10-20 days ฿3,270.00

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tert-Butyl (4-chloropyridin-2-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It serves as a protected amine building block in medicinal chemistry, enabling selective reactions at other functional sites during multi-step syntheses. Commonly employed in the preparation of bioactive molecules targeting inflammatory and oncological pathways. Its stability under various reaction conditions makes it valuable in solid-phase and solution-phase peptide-like synthesis

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. It serves as a protected amine building block in medicinal chemistry, enabling selective reactions at other functional sites during multi-step syntheses. Commonly employed in the preparation of bioactive molecules targeting inflammatory and oncological pathways. Its stability under various reaction conditions makes it valuable in solid-phase and solution-phase peptide-like synthesis. Also utilized in agrochemical research for constructing nitrogen-containing heterocycles with pesticidal activity.

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