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Structure of 391624-66-1
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This chiral diester features two (2-methylbenzoyl) ester groups at the 2 and 3 positions of a succinic acid backbone, enabling selective derivatization in asymmetric synthesis. The ortho-methyl substitution enhances steric control during enantioselective transformations.
(2S,3S)-2,3-Bis((2-methylbenzoyl)oxy)succinic acid serves as a chiral auxiliary in asymmetric synthesis, enabling stereocontrolled functionalization through its rigid, well-defined stereocenters. The molecule’s benzoate ester groups provide excellent bench stability and facilitate straightforward purification via crystallization. It functions effectively in diastereoselective transformations, particularly in enantioselective acylations and cyclizations, offering predictable stereochemical outcomes in the construction of complex molecular architectures.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: