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Structure of 2010973-00-7
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(R)-5-CF3-Pyox-iPr is a bench-stable, moisture-tolerant chiral pyridoxal analog featuring a trifluoromethyl group at the 5-position and an isopropyl substituent. This configuration enhances electron-withdrawing character and steric shielding, enabling selective coupling reactions in asymmetric synthesis workflows.
(R)-5-CF₃-Pyox-iPr serves as a robust chiral building block for the synthesis of fluorinated heterocycles, leveraging its trifluoromethyl-substituted pyridine core and stereogenic center. It facilitates efficient coupling reactions and functions reliably in transition-metal-catalyzed transformations, offering enhanced metabolic stability and lipophilicity. The isopropyl oxime group provides excellent bench stability and simplifies purification, making it well-suited for iterative synthesis in medicinal chemistry workflows.
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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: