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 1273655-83-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-6-methyl-2,3-dihydroinden-1-one features a sterically hindered, electron-deficient carbonyl scaffold ideal for transition-metal-catalyzed couplings. The bromine and methyl substituents enable selective functionalization in complex synthesis workflows, while the dihydroindenone core offers enhanced stability under standard conditions.
5-Bromo-6-methyl-2,3-dihydroinden-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indenones and heterocyclic scaffolds. The bromine atom facilitates palladium-catalyzed cross-coupling reactions, while the ketone functionality supports enolization and nucleophilic additions. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for medicinal chemistry applications and modular synthesis 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-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: