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 2207601-12-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(2S,2'S,3S,3'S)-DI-iPr-BABIBOP features a rigid, chiral bis(oxazoline) scaffold with diisopropyl substituents that enhance steric shielding and improve enantioselectivity in transition metal catalysis. This configuration delivers high stability and reproducible asymmetric induction in copper- and zinc-mediated reactions.
(2S,2'S,3S,3'S)-DI-iPr-BABIBOP serves as a chiral, bidentate ligand in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation with high enantioselectivity. Its sterically shielded diisopropyl substituents enhance catalyst stability and suppress undesired side reactions. The ligand demonstrates broad functional group tolerance and facilitates reliable coupling of aryl halides and pseudohalides under mild conditions, making it well-suited for complex molecule synthesis in medicinal chemistry and process development workflows.
|
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-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: