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 1260017-17-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-4-chloro-2,3-dihydro-1H-inden-1-one features a rigid indenone scaffold with complementary halogen substituents enabling diverse cross-coupling transformations. The bromine and chlorine atoms serve as distinct reactive handles for palladium-catalyzed coupling reactions, offering orthogonal functionalization potential in synthetic sequences. This molecule integrates readily into complex molecular architectures under standard conditions.
6-Bromo-4-chloro-2,3-dihydro-1H-inden-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indene scaffolds. Its orthogonal halogenation pattern facilitates selective cross-coupling reactions, while the ketone functionality supports nucleophilic additions and condensation processes. Bench-stable and amenable to standard purification methods, it functions reliably in multistep syntheses for pharmaceutical intermediates and functional materials.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P261-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: