(4R,4'R)-2,2'-(Cyclohexane-1,1-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)

97%, 99% e.e.

Reagent Code: #229234
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CAS Number 2757082-26-9

science Other reagents with same CAS 2757082-26-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.5 g/mol
Formula C₂₀H₃₄N₂O₂
badge Registry Numbers
MDL Number MFCD32201211
thermostat Physical Properties
Boiling Point 409.5±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.10±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organometallic reactions. Its rigid cyclohexane backbone and stereogenic centers enable high stereocontrol, making it valuable in the synthesis of optically active compounds such as pharmaceuticals and fine chemicals. Commonly employed in copper-catalyzed cyclopropanations, aldol reactions, and other transformations where precise chirality transfer is required. The tert-butyl groups enhance steric shielding, improving enantioselectivity. Often coordinated to metal centers to form active catalytic species in homogeneous systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,400.00
250mg
10-20 days ฿24,450.00
(4R,4'R)-2,2'-(Cyclohexane-1,1-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organometallic reactions. Its rigid cyclohexane backbone and stereogenic centers enable high stereocontrol, making it valuable in the synthesis of optically active compounds such as pharmaceuticals and fine chemicals. Commonly employed in copper-catalyzed cyclopropanations, aldol reactions, and other transformations where precise chirality transfer is required. The tert-butyl groups enhance steric shielding, improving enant

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organometallic reactions. Its rigid cyclohexane backbone and stereogenic centers enable high stereocontrol, making it valuable in the synthesis of optically active compounds such as pharmaceuticals and fine chemicals. Commonly employed in copper-catalyzed cyclopropanations, aldol reactions, and other transformations where precise chirality transfer is required. The tert-butyl groups enhance steric shielding, improving enantioselectivity. Often coordinated to metal centers to form active catalytic species in homogeneous systems.

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