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 29835-28-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-(3-Bromophenyl)propiolic acid features a conjugated alkyne tethered to a brominated phenyl ring, enabling direct incorporation into click chemistry workflows. The electron-deficient alkyne facilitates efficient copper-catalyzed azide-alkyne cycloaddition, while the ortho-bromine group supports subsequent palladium-mediated functionalization. This dual-reactive scaffold streamlines access to complex molecular architectures in medicinal chemistry and materials science.
3-(3-Bromophenyl)propiolic acid serves as a versatile building block for constructing functionalized aromatic alkynes, enabling efficient Sonogashira coupling and heterocycle synthesis. Its conjugated alkyne functionality exhibits robust stability under standard bench conditions and tolerates diverse reaction environments. The ortho-bromo substituent facilitates further transition-metal-catalyzed transformations, including cross-coupling and cyclization reactions, making it valuable for the modular assembly of complex scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: