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Structure of 1926162-97-1
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This (R)-configured fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered tert-pentyl ether group that enhances stability and solubility. The electron-deficient carbonyl moiety enables efficient coupling reactions, while the chiral center ensures enantioselective incorporation in peptide synthesis workflows under standard conditions.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((3-methylpentan-3-yl)oxy)-4-oxobutanoic acid serves as a versatile chiral building block for the synthesis of β-lactam antibiotics and peptidomimetics. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient solid-phase peptide synthesis, while the tert-pentyl ether moiety provides steric protection and enhanced bench stability. This compound facilitates orthogonal functionalization in multi-step sequences and is compatible with standard deprotection protocols.
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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: