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Structure of 57213-48-6
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H-Phe(3-CN)-OH is a synthetically accessible phenylalanine derivative featuring a para-cyano substituent on the aromatic ring. This electron-deficient aryl group enhances reactivity in coupling reactions and improves metabolic stability. The carboxylic acid terminus enables direct incorporation into peptides without additional protection, streamlining synthesis workflows in medicinal chemistry and peptide library development.
H-Phe(3-CN)-OH serves as a versatile building block for peptide synthesis, featuring a meta-cyano substitution on the phenyl ring that enhances electronic modulation and metabolic stability. The cyano group enables subsequent transformations such as amidation or hydrolysis to carboxylic acid derivatives, while maintaining compatibility with standard Fmoc-based solid-phase protocols. Bench-stable and readily purified by recrystallization or chromatography, it facilitates efficient access to bioactive peptides and heterocyclic scaffolds in medicinal chemistry campaigns.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 3439
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H332
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: