(R)-2-(2-((S)-(4-(tert-Butyl)phenyl)sulfinyl)phenyl)-4-phenyl-4,5-dihydrooxazole

98%

Reagent Code: #231291
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CAS Number 1965335-75-4

science Other reagents with same CAS 1965335-75-4

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in asymmetric synthesis as a chiral auxiliary or ligand in enantioselective catalytic reactions. Its rigid oxazoline-sulfinyl scaffold enables high stereocontrol, particularly in carbon–carbon bond-forming reactions such as aldol additions or cycloadditions. Commonly employed in pharmaceutical research to prepare enantiomerically pure intermediates, especially in the development of bioactive molecules where stereochemistry is critical. Soluble in common organic solvents, it facilitates homogeneous reaction conditions and is often recovered and reused in industrial processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,730.00
250mg
10-20 days ฿16,780.00
1g
10-20 days ฿50,470.00
(R)-2-(2-((S)-(4-(tert-Butyl)phenyl)sulfinyl)phenyl)-4-phenyl-4,5-dihydrooxazole
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Used in asymmetric synthesis as a chiral auxiliary or ligand in enantioselective catalytic reactions. Its rigid oxazoline-sulfinyl scaffold enables high stereocontrol, particularly in carbon–carbon bond-forming reactions such as aldol additions or cycloadditions. Commonly employed in pharmaceutical research to prepare enantiomerically pure intermediates, especially in the development of bioactive molecules where stereochemistry is critical. Soluble in common organic solvents, it facilitates homogeneous r

Used in asymmetric synthesis as a chiral auxiliary or ligand in enantioselective catalytic reactions. Its rigid oxazoline-sulfinyl scaffold enables high stereocontrol, particularly in carbon–carbon bond-forming reactions such as aldol additions or cycloadditions. Commonly employed in pharmaceutical research to prepare enantiomerically pure intermediates, especially in the development of bioactive molecules where stereochemistry is critical. Soluble in common organic solvents, it facilitates homogeneous reaction conditions and is often recovered and reused in industrial processes.

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