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 2173637-20-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Lithium (S)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate is a bench-stable, enantiomerically pure aziridine derivative featuring a protected chiral nitrogen center. This reagent integrates seamlessly into asymmetric synthesis workflows, enabling stereoselective ring-opening reactions and serving as a key building block for complex heterocyclic architectures in medicinal chemistry and natural product synthesis.
Lithium (S)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate serves as a stable, bench-ready chiral building block for the synthesis of β-amino acid derivatives and nitrogen-containing heterocycles. Its aziridine core enables regioselective ring-opening reactions with nucleophiles, while the Boc-protected amine and carboxylate functionalities offer orthogonal reactivity. The lithium counterion enhances solubility and reactivity in polar solvents, facilitating efficient transformations under mild conditions. This compound is particularly valuable in the construction of biologically relevant scaffolds where stereocontrol and functional group compatibility are essential.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: