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Structure of 1690-75-1
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Methyl 1-methylpiperidine-4-carboxylate features a sterically hindered piperidine core with a methylated nitrogen and a pendant ester group. This configuration enhances solubility in organic solvents while maintaining stability under standard bench conditions. The molecule serves as a key intermediate in the synthesis of bioactive alkaloids and pharmaceutical candidates, particularly where modulated basicity and metabolic resistance are required.
Methyl 1-methylpiperidine-4-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds common in bioactive molecules. Its methyl ester group facilitates straightforward functionalization via hydrolysis or reduction, while the tertiary amine center offers robust compatibility with standard coupling and derivatization protocols. The compound exhibits excellent bench stability and ease of purification, making it well-suited for iterative synthesis campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS02,GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H225-H314
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Precautionary Statements : P210-P240-P241-P280-P370+P378
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Lot numbers can be found on the outside label of a product: