anti-1,2,2,3,4,4-Hexamethylphosphetane 1-Oxide

≥98%(GC)

Reagent Code: #195995
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CAS Number 33530-51-7

science Other reagents with same CAS 33530-51-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.22 g/mol
Formula C₉H₁₉OP
badge Registry Numbers
MDL Number MFCD32857307
thermostat Physical Properties
Boiling Point 263.7±7.0 °C
inventory_2 Storage & Handling
Density 0.93±0.1 g/cm3
Storage Room temperature

description Product Description

Used as a highly effective organocatalyst in asymmetric synthesis, particularly in enantioselective oxidation reactions. Its unique sterically hindered structure enhances selectivity and stability, making it valuable in the production of chiral intermediates for pharmaceuticals and fine chemicals. Commonly employed in the synthesis of bioactive molecules where precise stereochemical control is required. Also utilized in research settings to develop new catalytic pathways due to its robust performance under various reaction conditions.

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inventory 1g
10-20 days ฿6,200.00

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anti-1,2,2,3,4,4-Hexamethylphosphetane 1-Oxide
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Used as a highly effective organocatalyst in asymmetric synthesis, particularly in enantioselective oxidation reactions. Its unique sterically hindered structure enhances selectivity and stability, making it valuable in the production of chiral intermediates for pharmaceuticals and fine chemicals. Commonly employed in the synthesis of bioactive molecules where precise stereochemical control is required. Also utilized in research settings to develop new catalytic pathways due to its robust performance und

Used as a highly effective organocatalyst in asymmetric synthesis, particularly in enantioselective oxidation reactions. Its unique sterically hindered structure enhances selectivity and stability, making it valuable in the production of chiral intermediates for pharmaceuticals and fine chemicals. Commonly employed in the synthesis of bioactive molecules where precise stereochemical control is required. Also utilized in research settings to develop new catalytic pathways due to its robust performance under various reaction conditions.

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