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Structure of 1627185-88-9
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This tert-butyl ((3S,4S)-4-methoxypyrrolidin-3-yl)carbamate features a stereochemically defined pyrrolidine core with a methoxy group at the 4-position and a bench-stable tert-butyloxycarbonyl (Boc) protecting group. The configuration enhances its utility in asymmetric synthesis, where it serves as a chiral building block for complex nitrogen-containing scaffolds. Its solubility profile supports efficient coupling reactions under standard conditions.
tert-Butyl ((3S,4S)-4-methoxypyrrolidin-3-yl)carbamate serves as a stereochemically defined pyrrolidine building block, enabling efficient access to chiral nitrogen-containing scaffolds. The tert-butoxycarbonyl (Boc) group provides excellent stability and ease of removal under mild acidic conditions, while the 4-methoxy substituent enhances solubility and modulates reactivity in downstream transformations. This compound functions reliably in peptide coupling, alkylation, and transition-metal-catalyzed cross-coupling reactions, making it a practical choice for medicinal chemistry and process development 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: