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CAS 231958-14-8

:

6-[(tert-butoxycarbonyl)amino]pyridine-3-carboxylic acid

Description:
6-[(tert-Butoxycarbonyl)amino]pyridine-3-carboxylic acid is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of the tert-butoxycarbonyl (Boc) group indicates that this compound is likely used in peptide synthesis as a protecting group for amines, enhancing its utility in organic synthesis. The carboxylic acid functional group contributes to its acidity and potential for forming salts or participating in esterification reactions. This compound is typically a white to off-white solid and is soluble in polar organic solvents, making it suitable for various chemical reactions. Its structure allows for potential interactions with biological systems, which may be of interest in medicinal chemistry. The CAS number 231958-14-8 uniquely identifies this compound, facilitating its recognition in chemical databases and literature. Overall, its functional groups and structural features make it a versatile intermediate in synthetic organic chemistry.
Formula:C11H14N2O4
InChI:InChI=1/C11H14N2O4/c1-11(2,3)17-10(16)13-8-5-4-7(6-12-8)9(14)15/h4-6H,1-3H3,(H,14,15)(H,12,13,16)
SMILES:CC(C)(C)OC(=Nc1ccc(cn1)C(=O)O)O
Synonyms:
  • 3-Pyridinecarboxylic Acid, 6-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-
  • 6-[(tert-Butoxycarbonyl)amino]nicotinic acid
  • 6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-3-carboxylic acid
  • 6-[(tert-Butoxycarbonyl)amino]pyridine-3-carboxylic acid, 2-[(tert-Butoxycarbonyl)amino]-5-carboxypyridine
  • 6-{[(tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid
  • 6-Aminonicotinic acid, 6-BOC protected
  • 6-Aminonicotinic acid, N-BOC protected
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