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 149506-35-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Dimethyl 2-(4-bromophenyl)malonate features a brominated phenyl group flanking a malonate ester core, enabling direct incorporation into cross-coupling reactions. This bench-stable derivative delivers high functional group tolerance and facilitates the synthesis of biaryl architectures under standard conditions.
Dimethyl 2-(4-bromophenyl)malonate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromoaryl functionality. The malonate ester moiety facilitates facile deprotonation and subsequent alkylation or cyclization, supporting the construction of biologically relevant heterocycles and substituted aromatic systems. Its bench stability and ease of purification make it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: