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Structure of 507472-08-4
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This fluorenylmethoxycarbonyl-protected thiophene-containing amino acid features a bench-stable, moisture-tolerant side chain ideal for peptide synthesis. The β-thiophenepropanoic acid scaffold integrates readily into peptide backbones, while the Fmoc group enables orthogonal deprotection. This derivative supports efficient solid-phase and solution-phase coupling protocols.
(βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-thiophenepropanoic acid serves as a chiral building block for peptide synthesis, enabling the incorporation of thiophene-containing amino acids with defined stereochemistry. The Fmoc group provides orthogonal protection and facilitates efficient removal under mild basic conditions. Its stability, compatibility with standard coupling reagents, and ease of purification make it ideal for solid-phase and solution-phase peptide assembly workflows.
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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: