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Structure of 61278-21-5
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(S)-3-aminopropane-1,2-diol features a chiral center with defined stereochemistry, enabling precise incorporation into bioactive molecules. This hydroxylated amine scaffold delivers enhanced solubility and hydrogen-bonding capacity, supporting efficient integration in peptide mimetics and kinase inhibitor design under standard bench conditions.
(S)-3-Aminopropane-1,2-diol serves as a key chiral building block for the synthesis of bioactive heterocycles and amino acid derivatives. Its three contiguous functional groups—primary amine, primary alcohol, and secondary alcohol—enable diverse transformations under standard conditions. The molecule exhibits excellent bench stability and facilitates efficient derivatization with minimal protection requirements, making it well-suited for modular synthetic sequences in medicinal chemistry and process development workflows.
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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 : Ⅱ
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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: