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Structure of 266318-79-0
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N-Fmoc-(S)-3-amino-4-methylpentanoic acid features a chiral, side-chain-functionalized amino acid scaffold with a bulky methyl substituent. This configuration enhances steric differentiation in peptide synthesis, while the Fmoc group enables efficient N-terminal protection and orthogonal deprotection. The pendant amine facilitates conjugation or branching in macrocyclic and peptidomimetic architectures.
N-Fmoc-(S)-3-amino-4-methylpentanoic acid serves as a versatile building block for peptide synthesis and medicinal chemistry applications. The Fmoc group enables efficient orthogonal protection during solid-phase peptide coupling, while the (S)-configured amino group and branched aliphatic side chain provide structural diversity for bioactive molecule design. Its bench-stable nature and compatibility with standard deprotection protocols facilitate reliable incorporation into complex scaffolds.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: