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Structure of 181289-33-8
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(R)-3-(2-Amino-2-oxoethyl)-5-methylhexanoic acid serves as a chiral building block for peptide-based drug discovery, enabling the synthesis of bioactive peptidomimetics. Its α-amino ketone functionality facilitates reductive amination and condensation reactions under standard conditions, while the stereogenic center ensures high diastereoselectivity in downstream transformations. The molecule exhibits good bench stability and is amenable to purification via standard chromatographic methods, supporting scalable synthesis in medicinal chemistry workflows.
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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: