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Structure of 70684-84-3
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This tetrahydropyridine derivative features a tert-butyl carbamate-protected amine and a carboxylic acid group, enabling direct incorporation into peptide backbones or as a building block in heterocyclic synthesis. The protected nitrogen enhances stability during reaction sequences, while the electron-deficient ring facilitates selective functionalization.
1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridine-4-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine and piperidine scaffolds. Its bench-stable tert-butyl ester and carboxylic acid functionalities offer orthogonal reactivity, facilitating selective derivatization and coupling reactions. Functions as a key intermediate in the construction of bioactive molecules through standard peptide coupling, hydrogenation, and functional group interconversions.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P405-P501
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Lot numbers can be found on the outside label of a product: