TETRABUTYLAMMONIUM CYANATE

Reagent Code: #242387
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CAS Number 39139-87-2

science Other reagents with same CAS 39139-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.48 g/mol
Formula C₁₇H₃₆N₂O
badge Registry Numbers
MDL Number MFCD00043222
thermostat Physical Properties
Melting Point 86-88 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inflatable

description Product Description

Used as a phase-transfer catalyst in organic synthesis, facilitating reactions between reagents in different phases by transferring ions into organic solvents. Commonly employed in the preparation of ureas, carbamates, and other nitrogen-containing compounds due to its ability to deliver cyanate ions under mild conditions. Also utilized in the synthesis of peptides and heterocyclic compounds where controlled nucleophilic addition is required. Its solubility in both aqueous and organic media makes it effective in biphasic reaction systems.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,890.00
inventory 5g
10-20 days ฿34,990.00

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TETRABUTYLAMMONIUM CYANATE
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Used as a phase-transfer catalyst in organic synthesis, facilitating reactions between reagents in different phases by transferring ions into organic solvents. Commonly employed in the preparation of ureas, carbamates, and other nitrogen-containing compounds due to its ability to deliver cyanate ions under mild conditions. Also utilized in the synthesis of peptides and heterocyclic compounds where controlled nucleophilic addition is required. Its solubility in both aqueous and organic media makes it effe

Used as a phase-transfer catalyst in organic synthesis, facilitating reactions between reagents in different phases by transferring ions into organic solvents. Commonly employed in the preparation of ureas, carbamates, and other nitrogen-containing compounds due to its ability to deliver cyanate ions under mild conditions. Also utilized in the synthesis of peptides and heterocyclic compounds where controlled nucleophilic addition is required. Its solubility in both aqueous and organic media makes it effective in biphasic reaction systems.

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