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Structure of 188792-67-8
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This piperidine derivative features a tert-butoxycarbonyl-protected amine and an ethyl-substituted carboxylic acid, enabling direct incorporation into peptide synthesis. The protected nitrogen facilitates sequential coupling without side reactions, while the electron-rich piperidine ring enhances solubility under standard conditions.
1-(tert-Butoxycarbonyl)-4-ethylpiperidine-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of piperidine-based scaffolds through straightforward deprotection and functionalization. The tert-butyl carbamate group offers excellent stability under basic conditions and facilitates selective N-alkylation or amide coupling reactions. Its ethyl-substituted piperidine core provides defined stereochemistry and enhanced lipophilicity, making it valuable for optimizing pharmacokinetic properties in API development.
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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: