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Structure of 59234-40-1
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rel-(2R,6S)-Piperidine-2,6-dicarboxylic acid is a stereochemically defined piperidine scaffold featuring two carboxylic acid groups at the 2 and 6 positions. This configuration imparts distinct conformational rigidity and polarity, enabling its use as a key building block in the synthesis of bioactive molecules and peptidomimetics. The molecule demonstrates enhanced solubility and stability under standard bench conditions.
rel-(2R,6S)-Piperidine-2,6-dicarboxylic acid serves as a stereochemically defined building block for the synthesis of bioactive heterocycles and peptidomimetics. Its rigid, chiral piperidine core enables precise control over molecular conformation in medicinal chemistry applications. The dicarboxylic acid functionality offers versatile handles for derivatization, including amide coupling and salt formation, while maintaining bench stability and compatibility with standard purification techniques.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: