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 82044-23-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-Oxirane-2-carboxylate (potassium) delivers a chiral epoxide moiety with high enantioselectivity in asymmetric synthesis. This bench-stable, moisture-tolerant reagent integrates readily into catalytic cycles, enabling stereoselective ring-opening reactions under mild conditions. Its potassium counterion enhances solubility in polar solvents while maintaining structural integrity.
(R)-Oxirane-2-carboxylate (potassium) serves as a chiral building block for asymmetric synthesis, enabling stereoselective ring-opening reactions with nucleophiles. Its bench-stable nature and high enantiomeric purity facilitate reliable access to functionalized β-hydroxy esters and other synthetically valuable intermediates in medicinal chemistry and natural product synthesis.
|
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-P280-P304+P340-P405
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: