(4S,4'S)-2,2'-(Cycloheptane-1,1-diyl)bis(4-benzyl-4,5-dihydrooxazole)

97%

Reagent Code: #237874
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CAS Number 2757082-25-8

science Other reagents with same CAS 2757082-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 416.55 g/mol
Formula C₂₇H₃₂N₂O₂
badge Registry Numbers
MDL Number MFCD32670842
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as alkylations, aldol reactions, and cycloadditions. Its rigid cycloheptane backbone and oxazoline rings provide a well-defined chiral environment, enhancing stereocontrol in metal-catalyzed reactions. Commonly employed with metals like copper, nickel, or palladium to achieve high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals.

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inventory 100mg
10-20 days ฿4,550.00

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(4S,4'S)-2,2'-(Cycloheptane-1,1-diyl)bis(4-benzyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as alkylations, aldol reactions, and cycloadditions. Its rigid cycloheptane backbone and oxazoline rings provide a well-defined chiral environment, enhancing stereocontrol in metal-catalyzed reactions. Commonly employed with metals like copper, nickel, or palladium to achieve high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals.

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as alkylations, aldol reactions, and cycloadditions. Its rigid cycloheptane backbone and oxazoline rings provide a well-defined chiral environment, enhancing stereocontrol in metal-catalyzed reactions. Commonly employed with metals like copper, nickel, or palladium to achieve high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals.

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