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tert-butyl 2-oxo-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate
$600.00
CAS No.: 1250999-73-5
Catalog No.: 195215
Purity: 95%
MF: C12H19NO4
MW: 241.287
Storage: 2-8 degree Celsius
SMILES: O=C1CC2(C1)OCCN(C2)C(=O)OC(C)(C)C
Catalog No.: 195215
Purity: 95%
MF: C12H19NO4
MW: 241.287
Storage: 2-8 degree Celsius
SMILES: O=C1CC2(C1)OCCN(C2)C(=O)OC(C)(C)C
tert-butyl 2-oxo-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate; CAS No.: 1250999-73-5; tert-butyl 2-oxo-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate. PROPERTIES: tert-butyl 2-oxo-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate appears as a white to off-white crystalline powder with a slight odor. Its molecular formula is C12H19NO5, corresponding to a molecular weight of approximately 261.3 g/mol. The compound exhibits a melting point in the range of 120-123 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: tert-butyl 2-oxo-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate serves as a specialized intermediate in the synthesis of bioactive molecules. Its spirocycle and oxo group provide structural features important for forming coordination complexes and catalytic systems used in asymmetric synthesis. In pharmaceutical research, it functions as a building block for creating anticancer agents and kinase inhibitors, leveraging its structural similarity to natural nucleotides to enable selective targeting of protein kinases. Additionally, the compound finds application in the development of fluorescent probes for bioimaging, where its oxo group allows for selective labeling of biological targets. It is also employed in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings.
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