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Structure of 68947-43-3
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1-Methylpiperidine-4-carboxylic acid features a sterically hindered piperidine core with a carboxylic acid group at the 4-position, enabling efficient incorporation into peptide-like scaffolds. The N-methyl substitution enhances metabolic stability and modulates solubility, while the acidic functionality facilitates conjugation and salt formation under standard conditions.
1-Methylpiperidine-4-carboxylic acid serves as a versatile scaffold in medicinal chemistry, enabling the construction of bioactive heterocycles and peptidomimetics. Its well-defined stereochemistry and amide-forming capability facilitate efficient incorporation into lead compounds. The molecule exhibits favorable bench stability and compatibility with standard coupling protocols, supporting scalable synthesis and purification via common chromatographic methods.
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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
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: