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Structure of 179747-84-3
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Benzyl(R)-(2,5-dioxopyrrolidin-3-yl)carbamate serves as a chiral auxiliary in asymmetric synthesis, featuring a pyrrolidinone core that enables stereocontrolled functionalization. The benzyl carbamate group provides stable protection for amine intermediates under standard conditions, facilitating sequential transformations with minimal racemization. This structure combines robustness with precise spatial control, making it ideal for complex molecule assembly.
Benzyl (R)-2,5-dioxopyrrolidin-3-yl carbamate serves as a robust chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations via its stable pyrrolidine scaffold. The carbamate group facilitates easy handling and purification, while the benzyl protecting group ensures orthogonal deprotection under mild conditions. This compound functions effectively in enantioselective alkylation and conjugate addition reactions, offering high diastereoselectivity and compatibility with diverse functional groups.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: