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Structure of 186320-06-9
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Fmoc-3-Ala(3-thienyl)-OH integrates a 3-thienyl-substituted alanine moiety with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct incorporation into peptide chains via standard solid-phase synthesis. The thienyl ring imparts enhanced electronic delocalization and steric profile, improving backbone rigidity and solubility in organic solvents. This derivative facilitates the construction of biologically active peptides featuring aromatic side chains with tailored conformational and physicochemical properties.
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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: