(4S)-4-(sec-Butyl)-2-(pyridin-2-yl)-4, 5-dihydrooxazole
98%
Reagent
Code: #236531
CAS Number
1620588-66-0
science Other reagents with same CAS 1620588-66-0
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Molecular Information
Weight
204.27 g/mol
Formula
C₁₂H₁₆N₂O
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Registry Numbers
MDL Number
MFCD34563669
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Storage & Handling
Storage
2-8°C, dry, light-proof
description Product Description
Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically enriched compounds. Its oxazoline core coordinates effectively with metal catalysts, making it valuable in catalytic asymmetric reactions such as aldol additions, alkylations, and Diels-Alder reactions. Commonly employed in pharmaceutical synthesis where stereochemical control is critical. The sec-butyl group enhances stereoselectivity due to its steric bulk, improving the efficiency of asymmetric induction. Also utilized in the development of ligands for transition-metal-catalyzed transformations.
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