Pyridine,5-isocyanato-2-[(tetrahydro-2H-pyran-4-yl)oxy]-

95%

Reagent Code: #223429
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CAS Number 912569-54-1

science Other reagents with same CAS 912569-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.2246 g/mol
Formula C₁₁H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD09702387
thermostat Physical Properties
Melting Point 68.5-70.5 °C
Boiling Point 342.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its isocyanate functional group readily reacts with amines and alcohols, making it valuable for constructing urea and carbamate linkages in drug molecules. The presence of the tetrahydropyranyl ether group enhances solubility and stability, which is beneficial in medicinal chemistry for improving pharmacokinetic properties. Commonly employed in research settings for the preparation of targeted therapies, including anticancer and anti-inflammatory agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿64,000.00

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Pyridine,5-isocyanato-2-[(tetrahydro-2H-pyran-4-yl)oxy]-
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its isocyanate functional group readily reacts with amines and alcohols, making it valuable for constructing urea and carbamate linkages in drug molecules. The presence of the tetrahydropyranyl ether group enhances solubility and stability, which is beneficial in medicinal chemistry for improving pharmacokinetic properties. Commonly employed in rese

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its isocyanate functional group readily reacts with amines and alcohols, making it valuable for constructing urea and carbamate linkages in drug molecules. The presence of the tetrahydropyranyl ether group enhances solubility and stability, which is beneficial in medicinal chemistry for improving pharmacokinetic properties. Commonly employed in research settings for the preparation of targeted therapies, including anticancer and anti-inflammatory agents.

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