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

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Reagent Code: #141678
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CAS Number 220270-49-5

science Other reagents with same CAS 220270-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 328.7912 g/mol
Formula C₁₅H₂₁ClN₂O₄
badge Registry Numbers
MDL Number MFCD16987738
thermostat Physical Properties
Boiling Point 402.6±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.210±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a protected intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The tert-butoxycarbonyl (Boc) group provides amine protection during peptide coupling or heterocyclic assembly, allowing selective reactivity at other functional sites. The 2-chloropyridin-4-yl moiety serves as a versatile building block for cross-coupling reactions, enabling the introduction of pyridine-based pharmacophores. Commonly employed in multi-step organic syntheses where stability under varying reaction conditions and controlled deprotection are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,360.00
inventory 250mg
10-20 days ฿5,760.00
inventory 500mg
10-20 days ฿9,600.00
inventory 1g
10-20 days ฿14,400.00

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tert-Butyl (tert-butoxycarbonyl)(2-chloropyridin-4-yl)carbamate
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Used as a protected intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The tert-butoxycarbonyl (Boc) group provides amine protection during peptide coupling or heterocyclic assembly, allowing selective reactivity at other functional sites. The 2-chloropyridin-4-yl moiety serves as a versatile building block for cross-coupling reactions, enabling the introduction of pyridine-based pharmacophores. Commonly

Used as a protected intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. The tert-butoxycarbonyl (Boc) group provides amine protection during peptide coupling or heterocyclic assembly, allowing selective reactivity at other functional sites. The 2-chloropyridin-4-yl moiety serves as a versatile building block for cross-coupling reactions, enabling the introduction of pyridine-based pharmacophores. Commonly employed in multi-step organic syntheses where stability under varying reaction conditions and controlled deprotection are required.

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