2,2,6,6-Tetramethylmorpholine

95%

Reagent Code: #242714
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CAS Number 19151-69-0

science Other reagents with same CAS 19151-69-0

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scatter_plot Molecular Information
Weight 143.23 g/mol
Formula C₈H₁₇NO
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MDL Number MFCD09897730
inventory_2 Storage & Handling
Storage 2-8°C, store away from light, dry seal

description Product Description

Used as a catalyst and reagent in organic synthesis, particularly in oxidation reactions. It is structurally analogous to the precursor of nitroxide radicals like TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) and can be employed in similar selective oxidation processes for converting alcohols to aldehydes or ketones. Also utilized in polymer chemistry as a stabilizer and catalyst in the production of polyurethanes. Its steric hindrance makes it effective in controlling reaction pathways and improving selectivity in complex syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,210.00
inventory 250mg
10-20 days ฿15,200.00
inventory 1g
10-20 days ฿45,760.00

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2,2,6,6-Tetramethylmorpholine
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Used as a catalyst and reagent in organic synthesis, particularly in oxidation reactions. It is structurally analogous to the precursor of nitroxide radicals like TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) and can be employed in similar selective oxidation processes for converting alcohols to aldehydes or ketones. Also utilized in polymer chemistry as a stabilizer and catalyst in the production of polyurethanes. Its steric hindrance makes it effective in controlling reaction pathways and improving selecti
Used as a catalyst and reagent in organic synthesis, particularly in oxidation reactions. It is structurally analogous to the precursor of nitroxide radicals like TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) and can be employed in similar selective oxidation processes for converting alcohols to aldehydes or ketones. Also utilized in polymer chemistry as a stabilizer and catalyst in the production of polyurethanes. Its steric hindrance makes it effective in controlling reaction pathways and improving selectivity in complex syntheses.
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