Methyl 5-{[(tert-butoxy)carbonyl]amino}-2-chloropyridine-4-carboxylate is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with a chlorine atom and a carboxylate group. The presence of the tert-butoxycarbonyl (Boc) group indicates that this compound is likely used in organic synthesis, particularly in the protection of amines during chemical reactions. The methyl ester functionality suggests that it can undergo hydrolysis to yield the corresponding carboxylic acid. This compound is typically utilized in pharmaceutical chemistry and may serve as an intermediate in the synthesis of biologically active molecules. Its properties, such as solubility and reactivity, are influenced by the electron-withdrawing nature of the chlorine atom and the steric bulk of the tert-butoxy group. Overall, this compound exemplifies the intricate design often found in synthetic organic chemistry, where specific functional groups are strategically incorporated to achieve desired reactivity and stability.

methyl 5-{[(tert-butoxy)carbonyl]amino}-2-chloropyridine-4-carboxylate

305371-42-0: Methyl 5-{[(tert-butoxy)carbonyl]amino}-2-chloropyridine-4-carboxylate is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with a chlorine atom and a carboxylate group. The presence of the tert-butoxycarbonyl (Boc) group indicates that this compound is likely used in organic synthesis, particularly in the protection of amines during chemical reactions. The methyl ester functionality suggests that it can undergo hydrolysis to yield the corresponding carboxylic acid. This compound is typically utilized in pharmaceutical chemistry and may serve as an intermediate in the synthesis of biologically active molecules. Its properties, such as solubility and reactivity, are influenced by the electron-withdrawing nature of the chlorine atom and the steric bulk of the tert-butoxy group. Overall, this compound exemplifies the intricate design often found in synthetic organic chemistry, where specific functional groups are strategically incorporated to achieve desired reactivity and stability.

4-Pyridinecarboxylic acid, 2-chloro-5-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester

<p>Methyl 5-{[(tert-butoxy)carbonyl]amino}-2-chloropyridine-4-carboxylate</p>

CAS 305371-42-0

methyl 5-{[(tert-butoxy)carbonyl]amino}-2-chloropyridine-4-carboxylate

4-Pyridinecarboxylic acid, 2-chloro-5-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester

Ref: IN-DA0030HL

Methyl 5-{[(tert-butoxy)carbonyl]amino}-2-chloropyridine-4-carboxylate

Ref: 54-OR1022232

METHYL 5-(BOC-AMINO)-2-CHLOROPYRIDINE-4-CARBOXYLATE

Ref: 10-F467411