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Structure of 851485-00-2
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trans-1-Boc-4-(4-chlorophenyl)-pyrrolidine-3-carboxylic acid features a sterically defined pyrrolidine core with a para-chlorophenyl substituent and a bench-stable Boc-protected carboxylic acid. This configuration enables direct incorporation into peptide scaffolds and complex heterocycles without racemization, offering reliable access to bioactive intermediates in medicinal chemistry workflows.
trans-1-Boc-4-(4-chlorophenyl)-pyrrolidine-3-carboxylic acid serves as a versatile chiral building block for medicinal chemistry campaigns, enabling the construction of pyrrolidine-based scaffolds with defined stereochemistry. The Boc group provides stable protection under standard reaction conditions, while the 4-chlorophenyl moiety offers orthogonal handle for further functionalization. Its bench-stable nature and compatibility with common coupling protocols facilitate efficient synthesis of bioactive molecules.
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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: