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Structure of 549532-08-3
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This chiral tert-butyl (R)-3-methoxypyrrolidine-1-carboxylate features a stereodefined pyrrolidine core with a bench-stable carbamate protecting group, enabling direct incorporation into asymmetric synthesis. The methoxy substituent enhances solubility and modulates electronic properties, facilitating efficient coupling reactions in medicinal chemistry applications.
tert-Butyl (R)-3-methoxypyrrolidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive nitrogen heterocycles. Its pyrrolidine core exhibits robust bench stability and tolerates diverse reaction conditions, enabling efficient functionalization at the 3-position. The tert-butyl carbamate group provides orthogonal protection compatible with standard deprotection protocols, facilitating downstream coupling and cyclization reactions in medicinal chemistry campaigns.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: