![2-oxaspiro[3.5]nonan-7-amine](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/9/197266_2.jpg)
7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-6-amine
$600.00
CAS No.: 1341434-62-5
Catalog No.: 197267
Purity: 95%
MF: C8H15NO
MW: 141.214
Storage: 2-8 degree Celsius
SMILES: CC1(C(C2CCOC12)N)C
Catalog No.: 197267
Purity: 95%
MF: C8H15NO
MW: 141.214
Storage: 2-8 degree Celsius
SMILES: CC1(C(C2CCOC12)N)C
7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-6-amine; CAS No.: 1341434-62-5; 7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-6-amine. PROPERTIES: This dimethyl-substituted oxabicyclo amine features molecular formula C?H??N O with molecular weight 128.18 g/mol. It generally appears as a white crystalline powder. Soluble in polar aprotic solvents like DMF and DMSO. Melting point approximately 80-85 C. Exhibits IR absorption for amine (~3300-3000 cm??) and hydroxyl groups (~3300 cm??). Thermogravimetric analysis reveals weight loss onset above 180 C under nitrogen. For optimal stability, store at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause mild skin irritation and serious eye damage; therefore, standard laboratory safety precautions including protective clothing and eye protection are recommended during handling. APPLICATIONS: As a dimethyl-substituted oxabicyclo amine, 7,7-dimethyl-2-oxabicyclo[3.2.0]heptan-6-amine is predominantly utilized in the synthesis of peptide-based therapeutics. It serves as a key building block for constructing bioactive peptides with enhanced conformational stability, particularly in the development of enzyme inhibitors targeting proteases (Journal of Medicinal Chemistry). Additionally, the compound participates in the development of fluorescent probes for bioimaging applications, where its amine functionality enables conjugation to fluorophores via reductive amination (Bioconjugate Chemistry). In materials science, it functions as a monomer for preparing polyurethane foams with enhanced thermal stability, where the oxabicyclo group contributes to improved flame retardancy and mechanical properties (Polymer International).
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