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 31501-85-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This cyclopropane carboxylic acid features a chiral (1R,2R) configuration and a para-bromophenyl substituent, delivering enhanced rigidity and defined stereochemistry. The brominated aromatic ring facilitates downstream functionalization, while the cyclopropane core imparts conformational constraint ideal for medicinal chemistry applications.
(1R,2R)-2-(4-Bromophenyl)cyclopropane-1-carboxylic acid serves as a valuable chiral building block for the synthesis of bioactive cyclopropanes and pharmaceutical intermediates. Its rigid bicyclic scaffold enables precise stereochemical control in asymmetric synthesis, while the pendant bromophenyl group facilitates downstream functionalization via palladium-catalyzed cross-coupling reactions. The carboxylic acid functionality offers versatility in derivatization and purification, enhancing its utility in medicinal chemistry campaigns.
|
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: