Octahydro-1H-indole-2-carboxylic acid
$300.00
CAS No.: 80828-13-3
Catalog No.: 196213
Purity: 95%
MF: C9H15NO2
MW: 169.224
Storage: 2-8 degree Celsius
SMILES: N1C(CC2CCCCC12)C(=O)O
Catalog No.: 196213
Purity: 95%
MF: C9H15NO2
MW: 169.224
Storage: 2-8 degree Celsius
SMILES: N1C(CC2CCCCC12)C(=O)O
Octahydro-1H-indole-2-carboxylic acid; CAS No.: 80828-13-3; Octahydro-1H-indole-2-carboxylic acid. PROPERTIES: This compound features an Octahydro-1H-indole-2-carboxylic acid structure, combining a fully hydrogenated indole ring system and a carboxylic acid group. It typically appears as a white to off-white crystalline solid with a molecular weight of approximately 169.2 g/mol (C9H17NO2). The melting point ranges between 150-155 C, and it exhibits moderate solubility in common organic solvents like ethanol, methanol, and ethyl acetate while being sparingly soluble in water. Proper storage requires a tightly sealed container in a cool, dry place. Safety considerations include wearing appropriate PPE. It is classified as a skin and eye irritant (GHS07) with the hazard statement H315-H319. APPLICATIONS: Octahydro-1H-indole-2-carboxylic acid serves as a valuable intermediate in pharmaceutical and chemical synthesis. Its Octahydro-1H-indole-2-carboxylic acid structure enables participation in various reactions, including esterification, amide bond formation, and nucleophilic substitution at the carboxylic acid group. In medicinal chemistry, it is used to develop bioactive molecules targeting the central nervous system and inflammatory pathways. The fully hydrogenated indole ring provides increased metabolic stability compared to aromatic indoles. This compound also functions as a building block in the synthesis of complex carbohydrates and glycosides. Academic studies employ it as a model compound in Medicinal Chemistry journals, focusing on optimizing the Octahydro-1H-indole-2-carboxylic acid scaffold for improved biological activity and pharmacokinetic properties.
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