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Structure of 122702-20-9
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(R)-2-Amino-3-hydroxypropanamide hydrochloride features a chiral α-amino acid scaffold with a hydroxyl group at the β-position, enabling precise stereochemical control in peptide synthesis. This bench-stable derivative integrates readily into peptidomimetic architectures and serves as a key building block for bioactive molecules requiring defined spatial orientation and hydrogen-bonding capacity.
(R)-2-Amino-3-hydroxypropanamide hydrochloride serves as a key chiral building block for synthesizing β-hydroxy amino acids and related pharmacophores. Its well-defined stereochemistry enables reliable incorporation into peptidomimetics and kinase inhibitor scaffolds. The compound exhibits good bench stability, facilitates straightforward purification via crystallization, and demonstrates compatibility with standard amine protection and coupling protocols in solid-phase synthesis.
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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: