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Structure of 870010-07-4
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Fmoc-3-Ala(5-thiazoyl)-OH features a 5-thiazoyl-modified alanine residue with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct incorporation into peptide chains. The thiazoyl moiety imparts enhanced solubility and stability under standard coupling conditions. This derivative serves as a key building block for synthesizing bioactive peptides containing sulfur-rich motifs.
Fmoc-3-Ala(5-thiazoyl)-OH serves as a versatile building block for peptide synthesis, enabling site-specific incorporation of a 5-thiazoyl-modified alanine residue. The Fmoc group ensures orthogonal protection for amine-directed coupling, while the thiazole moiety imparts enhanced rigidity and potential hydrogen-bonding capacity. This derivative exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard solid-phase and solution-phase 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: