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6-(tert-butoxycarbonyl)-6-azaspiro[3.5]nonane-2-carboxylic acid
$1,350.00
CAS No.: 1374659-03-6
Catalog No.: 195257
Purity: 95%
MF: C14H23NO4
MW: 269.341
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N1CC2(CC(C2)C(=O)O)CCC1
Catalog No.: 195257
Purity: 95%
MF: C14H23NO4
MW: 269.341
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N1CC2(CC(C2)C(=O)O)CCC1
6-(tert-butoxycarbonyl)-6-azaspiro[3.5]nonane-2-carboxylic acid; CAS No.: 1374659-03-6; 6-(tert-butoxycarbonyl)-6-azaspiro[3.5]nonane-2-carboxylic acid. PROPERTIES: 6-(tert-butoxycarbonyl)-6-azaspiro[3.5]nonane-2-carboxylic acid appears as a white to off-white crystalline powder with a slight odor. Its molecular formula is C13H21NO4, corresponding to a molecular weight of approximately 255.3 g/mol. The compound exhibits a melting point in the range of 140-145 C and demonstrates moderate solubility in common organic solvents such as methanol, ethyl acetate, and dichloromethane while being sparingly soluble in water. It is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: 6-(tert-butoxycarbonyl)-6-azaspiro[3.5]nonane-2-carboxylic acid functions as a valuable intermediate in the synthesis of pharmaceuticals. Its spirocycle and Boc-protected amine groups provide structural features important for forming stable conjugates with biological targets. In biochemical research, it serves as a building block for creating metabolites and signaling molecules involved in cellular processes. Additionally, it finds application in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings. The compound is also employed in the preparation of chiral ligands and catalysts used in asymmetric synthesis.
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