Isopropyl ((R)-(Perfluorophenoxy)(Phenoxy)Phosphoryl)-D-Alaninate

96%

Reagent Code: #200939
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CAS Number 1627824-09-2

science Other reagents with same CAS 1627824-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 453.3 g/mol
Formula C₁₈H₁₇F₅NO₅P
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral organophosphorus compound in asymmetric synthesis, particularly in the development of enantioselective catalysts and bioactive molecules. Its structure allows it to act as a phosphorylating agent in stereoselective reactions, making it valuable in pharmaceutical research for creating optically active intermediates. The presence of fluorinated and aromatic groups enhances its stability and influences reactivity, enabling use in specialized agrochemicals and medicinal chemistry applications where high selectivity and metabolic resistance are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,700.00
inventory 250mg
10-20 days ฿12,790.00
inventory 1g
10-20 days ฿31,380.00
Isopropyl ((R)-(Perfluorophenoxy)(Phenoxy)Phosphoryl)-D-Alaninate
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Used as a chiral organophosphorus compound in asymmetric synthesis, particularly in the development of enantioselective catalysts and bioactive molecules. Its structure allows it to act as a phosphorylating agent in stereoselective reactions, making it valuable in pharmaceutical research for creating optically active intermediates. The presence of fluorinated and aromatic groups enhances its stability and influences reactivity, enabling use in specialized agrochemicals and medicinal chemistry applications w
Used as a chiral organophosphorus compound in asymmetric synthesis, particularly in the development of enantioselective catalysts and bioactive molecules. Its structure allows it to act as a phosphorylating agent in stereoselective reactions, making it valuable in pharmaceutical research for creating optically active intermediates. The presence of fluorinated and aromatic groups enhances its stability and influences reactivity, enabling use in specialized agrochemicals and medicinal chemistry applications where high selectivity and metabolic resistance are required.
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