(S)-(+)-N-TBOC-2-methylpiperidine is a chiral amine that is commonly used in organic synthesis, particularly in the preparation of pharmaceuticals and other biologically active compounds. The "TBOC" (tert-butyloxycarbonyl) group serves as a protective group for the amine, facilitating various chemical reactions by preventing unwanted side reactions. This compound features a piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle, and the presence of a methyl group at the 2-position contributes to its steric and electronic properties. The chirality of the molecule, indicated by the (S)- designation, is crucial for its biological activity, as enantiomers can exhibit significantly different behaviors in biological systems. In terms of physical properties, (S)-(+)-N-TBOC-2-methylpiperidine is typically a colorless to pale yellow liquid or solid, depending on its form, and is soluble in organic solvents. Its applications extend to the synthesis of various compounds in medicinal chemistry, where the control of stereochemistry is essential for achieving desired pharmacological effects.

(S)-(+)-N-TBOC-2-METHYLPIPERIDINE

183903-99-3: (S)-(+)-N-TBOC-2-methylpiperidine is a chiral amine that is commonly used in organic synthesis, particularly in the preparation of pharmaceuticals and other biologically active compounds. The "TBOC" (tert-butyloxycarbonyl) group serves as a protective group for the amine, facilitating various chemical reactions by preventing unwanted side reactions. This compound features a piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle, and the presence of a methyl group at the 2-position contributes to its steric and electronic properties. The chirality of the molecule, indicated by the (S)- designation, is crucial for its biological activity, as enantiomers can exhibit significantly different behaviors in biological systems. In terms of physical properties, (S)-(+)-N-TBOC-2-methylpiperidine is typically a colorless to pale yellow liquid or solid, depending on its form, and is soluble in organic solvents. Its applications extend to the synthesis of various compounds in medicinal chemistry, where the control of stereochemistry is essential for achieving desired pharmacological effects.

CAS 183903-99-3

(S)-(+)-N-TBOC-2-METHYLPIPERIDINE

(S)-(+)-N-(Boc)-2-methylpiperidine

Ref: IN-DA003CHZ

tert-Butyl (S)-2-methylpiperidine-1-carboxylate

Ref: 54-OR321327