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Structure of 172695-22-6
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Tert-butyl (S)-(1-cyanopropan-2-yl)carbamate is a chiral building block featuring a stereodefined cyanopropyl moiety and a bench-stable tert-butoxycarbonyl (Boc) protecting group. This configuration enables direct incorporation into asymmetric synthesis, particularly in the construction of enantiopure amine derivatives. The nitrile group offers versatility for downstream functionalization, including hydrolysis to carboxylic acids or reductive conversion to primary amines. Its stability under standard conditions simplifies handling in process development workflows.
Tert-butyl (S)-(1-cyanopropan-2-yl)carbamate serves as a chiral building block for the synthesis of β-amino nitriles and functionalized heterocycles. Its stability under standard reaction conditions enables reliable use in asymmetric synthesis, while the tert-butyl carbamate group facilitates straightforward deprotection. The molecule functions effectively in nucleophilic addition and coupling reactions, offering high diastereoselectivity in peptide-like scaffold construction.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: