(4S,4'S)-Diisopropyl 2,2'-(cyclopropane-1,1-diyl)bis(4,5-dihydrooxazole-4-carboxylate)

95%

Reagent Code: #236855
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CAS Number 2328083-86-7

science Other reagents with same CAS 2328083-86-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.38 g/mol
Formula C₁₇H₂₄N₂O₆
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the stereocontrolled formation of complex organic molecules. Its rigid cyclopropane core and oxazoline rings provide a well-defined chiral environment, making it valuable in enantioselective transformations such as alkylations, aldol reactions, and Diels-Alder cyclizations. Commonly employed in pharmaceutical and fine chemical synthesis where high enantiomeric purity is required. The isopropyl ester groups allow for easy modification or removal after the desired reaction, facilitating efficient downstream processing.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,080.00
inventory 100mg
10-20 days ฿16,610.00
inventory 1g
10-20 days ฿90,080.00
inventory 250mg
10-20 days ฿29,700.00
(4S,4'S)-Diisopropyl 2,2'-(cyclopropane-1,1-diyl)bis(4,5-dihydrooxazole-4-carboxylate)
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Used as a chiral auxiliary in asymmetric synthesis, enabling the stereocontrolled formation of complex organic molecules. Its rigid cyclopropane core and oxazoline rings provide a well-defined chiral environment, making it valuable in enantioselective transformations such as alkylations, aldol reactions, and Diels-Alder cyclizations. Commonly employed in pharmaceutical and fine chemical synthesis where high enantiomeric purity is required. The isopropyl ester groups allow for easy modification or removal

Used as a chiral auxiliary in asymmetric synthesis, enabling the stereocontrolled formation of complex organic molecules. Its rigid cyclopropane core and oxazoline rings provide a well-defined chiral environment, making it valuable in enantioselective transformations such as alkylations, aldol reactions, and Diels-Alder cyclizations. Commonly employed in pharmaceutical and fine chemical synthesis where high enantiomeric purity is required. The isopropyl ester groups allow for easy modification or removal after the desired reaction, facilitating efficient downstream processing.

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