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 68076-39-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
N1,N5-Bis-Boc-spermidine features two Boc-protected amine groups, enabling stable, selective functionalization in peptide and polyamine synthesis. This bench-stable derivative simplifies the incorporation of spermidine scaffolds into complex molecular architectures under standard conditions.
N1,N5-Bis-Boc-spermidine serves as a key protected diamine building block for the synthesis of polyamine derivatives and functionalized heterocycles. The two Boc groups provide orthogonal protection of primary amines, enabling selective deprotection and stepwise coupling in multistep syntheses. Its bench-stable, crystalline nature facilitates handling and purification, while its compatibility with standard amide coupling and reductive amination protocols makes it well-suited for medicinal chemistry and macrocyclic scaffold construction.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: