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 1196154-87-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This cyclopenta[b]pyridinone derivative features a bromine substituent at the 3-position, enabling direct functionalization in cross-coupling reactions. The dihydroquinoline core provides a rigid, electron-deficient scaffold suitable for pharmaceutical and agrochemical synthesis. Bench-stable under standard conditions, it integrates readily into complex molecular architectures.
3-Bromo-6,7-dihydro-5H-cyclopenta[b]pyridin-5-one serves as a versatile building block in medicinal chemistry, enabling late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromo group exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the cyclic ketone moiety provides structural rigidity and hydrogen-bonding capability. Bench-stable and readily purified by flash chromatography, it functions effectively in multistep syntheses of heterocyclic scaffolds relevant to CNS-targeted therapeutics.
|
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: