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Structure of 177966-61-9
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzo[b]thiophen-3-yl)propanoic acid features a chiral α-amino acid scaffold bearing a fluorenylmethoxycarbonyl (Fmoc) protecting group and a sterically defined benzo[b]thiophene moiety. This configuration enables direct incorporation into peptide synthesis workflows, delivering high fidelity in sequence assembly under standard conditions. The Fmoc handle ensures orthogonal deprotection compatibility, while the aromatic thiophene side chain enhances solubility and structural rigidity for complex peptide architectures.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzo[b]thiophen-3-yl)propanoic acid serves as a robust chiral building block for peptide synthesis, leveraging the stability and orthogonal deprotection of the Fmoc group. Its benzo[b]thiophene moiety imparts structural rigidity and enhanced metabolic stability, facilitating efficient incorporation into bioactive scaffolds. The molecule exhibits excellent bench stability, clean reaction profiles, and compatibility with standard coupling protocols, enabling reliable access to complex peptide architectures in medicinal chemistry campaigns.
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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: