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Structure of 1359658-32-4
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tert-Butyl (R)-3-(methoxymethyl)piperazine-1-carboxylate features a chiral piperazine core with a methoxymethyl side chain and bench-stable tert-butyl carbamate protection. This configuration enables selective incorporation into complex scaffolds during peptide and small-molecule synthesis, particularly where stereocontrol and orthogonal functionality are required.
tert-Butyl (R)-3-(methoxymethyl)piperazine-1-carboxylate serves as a stable, bench-ready chiral building block for medicinal chemistry and process development. Its piperazine core enables efficient functionalization in standard coupling reactions, while the tert-butyl carbamate group offers orthogonal protection compatible with diverse synthetic sequences. The methoxymethyl substituent provides enhanced solubility and facilitates selective deprotection under mild acidic conditions, streamlining access to functionalized piperazine derivatives used in API synthesis.
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GHS Pictogram :
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GHS No : GHS07,GHS05
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Signal Word : Danger
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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-H318-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: