Imino-tris(dimethylamino)phosphorane

97%

Reagent Code: #76825
label
Alias N,N,N′,N′,N″,N″-Hexamethyl phosphoroimidotriamide; Phosphazene ligand P1-H
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CAS Number 49778-01-0

science Other reagents with same CAS 49778-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.22 g/mol
Formula C₆H₁₉N₄P
badge Registry Numbers
MDL Number MFCD00216725
inventory_2 Storage & Handling
Density 0.979 g/mL
Storage room temperature

description Product Description

Imino-tris(dimethylamino)phosphorane is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonation reactions, enabling the formation of carbanions and facilitating various condensation and cyclization processes. Its application is prominent in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where precise control over reactivity is essential. Additionally, it serves as a reagent in the preparation of phosphazenes and other phosphorus-containing compounds, which are valuable in materials science and catalysis. Its stability and strong basicity make it a preferred choice in reactions requiring harsh conditions or high selectivity.

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Test Parameter Specification
Purity 97-100%
Appearance colorless liquid

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,560.00

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Imino-tris(dimethylamino)phosphorane
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Imino-tris(dimethylamino)phosphorane is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonation reactions, enabling the formation of carbanions and facilitating various condensation and cyclization processes. Its application is prominent in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where precise control over reactivity is essential. Additionally, it serves as a reagent in the preparation of phosphaz

Imino-tris(dimethylamino)phosphorane is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonation reactions, enabling the formation of carbanions and facilitating various condensation and cyclization processes. Its application is prominent in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where precise control over reactivity is essential. Additionally, it serves as a reagent in the preparation of phosphazenes and other phosphorus-containing compounds, which are valuable in materials science and catalysis. Its stability and strong basicity make it a preferred choice in reactions requiring harsh conditions or high selectivity.

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