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Structure of 923012-40-2
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This fluoren-9-ylmethoxycarbonyl-protected chiral amino acid features a cyclopropyl group at the α-position, enhancing steric definition and metabolic stability. The (R)-configuration ensures enantioselective incorporation in peptide synthesis workflows. Designed for efficient coupling under standard conditions, this building block delivers high diastereoselectivity and compatibility with diverse reaction environments.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclopropylacetic acid serves as a valuable chiral building block in peptide synthesis, enabling the introduction of sterically hindered, cyclopropyl-containing amino acid residues. The Fmoc group provides orthogonal protection for primary amines, offering excellent stability under basic conditions and facilitating straightforward deprotection. Its well-defined stereochemistry and compatibility with standard coupling protocols make it ideal for solid-phase and solution-phase peptide assembly.
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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: