Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 1416176-14-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Boc-3-azaspiro[5.5]undecane-9-carbaldehyde features a rigid spirocyclic core with a protected tertiary amine and a reactive aldehyde handle. This configuration enables direct incorporation into diverse synthetic scaffolds, particularly in medicinal chemistry campaigns requiring constrained nitrogen-containing frameworks. The Boc group ensures stability during multi-step transformations, while the aldehyde facilitates conjugation via reductive amination or imine formation.
3-Boc-3-azaspiro[5.5]undecane-9-carbaldehyde serves as a versatile spirocyclic building block for medicinal chemistry, enabling efficient access to constrained heterocyclic scaffolds. The Boc-protected amine and aldehyde functionalities offer orthogonal reactivity for sequential functionalization, while the spirocyclic core imparts conformational rigidity. Its bench-stable nature and compatibility with standard coupling and reduction protocols facilitate streamlined synthesis of complex targets.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: