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Structure of 5267-64-1
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D-Penylalaninol features a chiral benzylic alcohol scaffold derived from D-phenylalanine, offering enhanced solubility and metabolic stability compared to parent amino acids. This hydroxylated analog integrates readily into peptide architectures, serving as a conformationally constrained residue that modulates backbone flexibility. Its aromatic side chain supports π–π interactions in target binding domains. The molecule exhibits bench-stable handling characteristics under standard conditions.
D-Penylalaninol serves as a valuable chiral building block in peptide synthesis and medicinal chemistry, offering a stable benzyl side chain with a primary alcohol functionality. Its well-defined stereochemistry enables stereoselective transformations, while the hydroxyl group facilitates derivatization or incorporation into bioactive scaffolds. The compound exhibits good bench stability and compatibility with standard protecting group strategies, making it suitable for multi-step synthetic sequences in API development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: