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tert-butyl 2-hydroxy-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate
$350.00
CAS No.: 2309427-24-3
Catalog No.: 195199
Purity: 95%
MF: C12H21NO4
MW: 243.303
Storage: 2-8 degree Celsius
SMILES: OC1CC2(C1)OCCN(C2)C(=O)OC(C)(C)C
Catalog No.: 195199
Purity: 95%
MF: C12H21NO4
MW: 243.303
Storage: 2-8 degree Celsius
SMILES: OC1CC2(C1)OCCN(C2)C(=O)OC(C)(C)C
tert-butyl 2-hydroxy-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate; CAS No.: 2309427-24-3; tert-butyl 2-hydroxy-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate. PROPERTIES: tert-butyl 2-hydroxy-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 C12H21NO5, corresponding to a molecular weight of approximately 263.3 g/mol. The compound exhibits a melting point in the range of 110-113 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-hydroxy-5-oxa-8-azaspiro[3.5]nonane-8-carboxylate serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the preparation of certain antiviral and anticancer agents. Its spirocycle and hydroxy groups provide structural features important for receptor binding and bioactivity. In medicinal chemistry, it functions as a building block for creating bioactive molecules, leveraging its ability to form stable conjugates with biological targets. Additionally, it finds application in the development of fluorescent probes for bioimaging, where its hydroxy and carboxylate groups allow for selective labeling of biological targets such as proteins and lipids. The compound is also employed in the synthesis of agrochemicals, though specific applications in this area are limited to non-agricultural research settings.
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