N-Benzyl-1-(trimethylsilyl)-N-((trimethylsilyl)methyl)methanamine

95%

Reagent Code: #214750
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CAS Number 144964-17-0

science Other reagents with same CAS 144964-17-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.57 g/mol
Formula C₁₅H₂₉NSi₂
badge Registry Numbers
MDL Number MFCD09834369
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a specialized reagent in organic synthesis, particularly in the preparation of silylated intermediates for pharmaceuticals and agrochemicals. Its dual trimethylsilyl groups enhance stability and solubility in nonpolar solvents, making it valuable in cross-coupling reactions and as a protecting group strategy. Commonly employed in the synthesis of complex amines and in lithiation processes where controlled reactivity is required. Also finds use in the development of silicon-containing functional materials and in catalysis research due to its unique steric and electronic properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿6,230.00
5g
10-20 days ฿21,780.00
N-Benzyl-1-(trimethylsilyl)-N-((trimethylsilyl)methyl)methanamine
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Used as a specialized reagent in organic synthesis, particularly in the preparation of silylated intermediates for pharmaceuticals and agrochemicals. Its dual trimethylsilyl groups enhance stability and solubility in nonpolar solvents, making it valuable in cross-coupling reactions and as a protecting group strategy. Commonly employed in the synthesis of complex amines and in lithiation processes where controlled reactivity is required. Also finds use in the development of silicon-containing functional m

Used as a specialized reagent in organic synthesis, particularly in the preparation of silylated intermediates for pharmaceuticals and agrochemicals. Its dual trimethylsilyl groups enhance stability and solubility in nonpolar solvents, making it valuable in cross-coupling reactions and as a protecting group strategy. Commonly employed in the synthesis of complex amines and in lithiation processes where controlled reactivity is required. Also finds use in the development of silicon-containing functional materials and in catalysis research due to its unique steric and electronic properties.

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