AA14581
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
50mg | 95% | in stock | $318.00 | $222.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA14581 |
Chemical Name: | tert-Butyl 1-oxo-2,6-diazaspiro[3.5]nonane-6-carboxylate |
CAS Number: | 1160246-71-8 |
Molecular Formula: | C12H20N2O3 |
Molecular Weight: | 240.2988 |
MDL Number: | MFCD12198505 |
SMILES: | O=C(N1CCCC2(C1)CNC2=O)OC(C)(C)C |
Complexity: | 348 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
Undefined Atom Stereocenter Count: | 1 |
XLogP3: | 0.5 |
6-Boc-1-oxo-2,6-diazaspiro[3.5]nonane, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis processes. Due to its unique structure and properties, this compound plays a crucial role in various organic synthesis applications.In chemical synthesis, 6-Boc-1-oxo-2,6-diazaspiro[3.5]nonane is frequently employed as a key building block for the synthesis of complex molecules. Its spirocyclic structure provides a rigid framework that can control molecular conformation and enhance the selectivity of chemical reactions. As a result, this compound serves as a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.Moreover, the Boc protecting group present in 6-Boc-1-oxo-2,6-diazaspiro[3.5]nonane offers a means to selectively mask certain reactive functional groups during synthesis, enabling chemists to carry out specific transformations without unwanted side reactions. This protective group can be easily removed under mild conditions, allowing for the subsequent modification of the molecule as needed.Overall, the strategic use of 6-Boc-1-oxo-2,6-diazaspiro[3.5]nonane in chemical synthesis allows for the efficient construction of intricate molecular structures with precise control over stereochemistry and functional group reactivity.