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Structure of 178119-93-2
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(4-hydroxyphenyl)acetic acid is a bench-stable, moisture-tolerant chiral building block featuring a fluorenylmethyl carbamate (Fmoc) protecting group. This configuration enables direct incorporation into peptide synthesis workflows, where the pendant phenolic hydroxyl supports downstream derivatization or conjugation.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(4-hydroxyphenyl)acetic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The Fmoc-protected amino group enables efficient coupling in solid-phase peptide synthesis, while the pendant phenolic hydroxyl offers a site for derivatization or orthogonal functionalization. Its bench-stable crystalline nature facilitates handling and purification, supporting scalable preparation of complex pharmaceutical intermediates.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: