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 1057217-63-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Bromo-2-quinolinecarboxylic acid features a bromine substituent at the 7-position of the quinoline scaffold, enhancing electrophilic reactivity and enabling direct functionalization in cross-coupling reactions. The carboxylic acid group provides a handle for derivatization, while the planar heteroaromatic core imparts stability and favorable solubility in polar organic solvents. This compound serves as a key intermediate in medicinal chemistry and materials synthesis.
7-Bromo-2-quinolinecarboxylic acid serves as a versatile building block for medicinal chemistry and materials science, enabling direct incorporation into biologically active heterocycles via standard coupling reactions. Its bromine and carboxylic acid functionalities provide orthogonal reactivity for palladium-catalyzed cross-couplings and amide bond formation, with excellent bench stability and straightforward purification.
|
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: