phenyl-(S)-4-phenyl-SUF-PYBOX

97%

Reagent Code: #233701
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CAS Number 2412796-38-2

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Weight 509.58 g/mol
Formula C₂₉H₂₃N₃O₄S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It forms complexes with metal ions such as copper(II), enabling highly stereoselective cyclopropanation, Diels-Alder, and aziridination reactions. Its rigid pyridine-bisoxazoline (PYBOX) framework enhances stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The phenyl and sulfonyl substituents fine-tune electronic and steric properties, improving catalyst performance and enantioselectivity in various C–C and C–heteroatom bond-forming reactions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿9,790.00
phenyl-(S)-4-phenyl-SUF-PYBOX
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It forms complexes with metal ions such as copper(II), enabling highly stereoselective cyclopropanation, Diels-Alder, and aziridination reactions. Its rigid pyridine-bisoxazoline (PYBOX) framework enhances stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The phenyl and sulfonyl substituents fine-tune electronic and steric properties, improvin

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It forms complexes with metal ions such as copper(II), enabling highly stereoselective cyclopropanation, Diels-Alder, and aziridination reactions. Its rigid pyridine-bisoxazoline (PYBOX) framework enhances stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The phenyl and sulfonyl substituents fine-tune electronic and steric properties, improving catalyst performance and enantioselectivity in various C–C and C–heteroatom bond-forming reactions.

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