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Structure of 142253-46-1
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1-Boc-3-(cyanomethyl)pyrrolidine features a pyrrolidine core bearing both a Boc-protected amine and a cyanomethyl substituent, enabling sequential functionalization in medicinal chemistry. The nitrile group offers a handle for derivatization via hydrolysis or nucleophilic addition, while the Boc moiety ensures stability during synthesis. This bifunctional scaffold supports rapid access to complex heterocyclic architectures under standard conditions.
1-Boc-3-(cyanomethyl)pyrrolidine serves as a versatile building block for the synthesis of pyrrolidine-based scaffolds in medicinal chemistry. The Boc group provides stability and orthogonal protection, while the cyanomethyl functionality enables downstream transformations such as nucleophilic addition, cyclization, or conversion to amide or carboxylic acid derivatives. Its bench-stable nature and compatibility with standard coupling and reduction protocols facilitate efficient access to complex heterocyclic 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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: