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*For research and further manufacturing use only, not for direct human use.
Structure of 2217-15-4
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(+)-Diisopropyl L-tartrate serves as a chiral auxiliary in asymmetric synthesis, enabling stereocontrolled transformations through its well-defined stereogenic centers. This bench-stable diester integrates readily into enantioselective reactions, delivering predictable stereochemical outcomes under standard conditions.
(+)-Diisopropyl L-tartrate serves as a well-established chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations through its defined stereochemistry. It functions effectively in enantioselective additions and epoxidations, offering high diastereoselectivity and bench stability. The compound's ease of purification and compatibility with standard reaction conditions make it a reliable choice for the construction of chiral building blocks in medicinal chemistry and natural product synthesis.
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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: