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Structure of 1416820-34-2
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(S)-4-CF3-Pyox-iPr is a bench-stable, moisture-tolerant chiral pyridine derivative featuring a trifluoromethyl group at the 4-position and an isopropyl substituent on the oxime nitrogen. This configuration enhances stereochemical control in asymmetric synthesis, enabling efficient coupling in transition-metal-catalyzed transformations and providing robust performance under standard reaction conditions.
(S)-4-CF₃-Pyox-iPr serves as a robust chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations through its stable pyrrolidine scaffold. The trifluoromethyl group enhances electronic polarization and metabolic stability, while the isopropyl substituent improves solubility and facilitates purification. This reagent reliably participates in standard amine alkylation, acylation, and conjugate addition reactions, offering high enantioselectivity and bench stability under ambient conditions.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: