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Structure of 2381854-90-4
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Fmoc-N-Me-3-(4-py)-L-Ala integrates a methoxy-substituted pyridyl group at the 3-position of L-alanine, enabling efficient conjugation in peptide synthesis. This derivative features enhanced solubility and stability under standard coupling conditions, facilitating rapid incorporation into complex sequences. The N-methylated amine prevents unwanted side reactions while maintaining compatibility with Fmoc-based protocols.
Fmoc-N-Me-3-(4-py)-L-Ala serves as a versatile building block in peptide synthesis, enabling the incorporation of a methylation-stabilized, 4-pyridyl-functionalized alanine residue. The Fmoc group ensures efficient orthogonal protection for amine-directed coupling, while the N-methyl substitution enhances metabolic stability and modulates conformational flexibility. The pendant pyridyl moiety provides a handle for downstream functionalization via metal-catalyzed cross-coupling or hydrogen bonding interactions, making it suitable for constructing bioactive peptide scaffolds and heterocyclic hybrids with predictable reactivity.
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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: