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 1211533-26-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-6-fluoronicotinic acid features a strategically positioned chloro and fluoro substituent on the nicotinic acid scaffold, delivering enhanced electronic effects and metabolic stability. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling efficient incorporation into bioactive molecules through amide coupling and Suzuki-Miyaura cross-coupling reactions under standard conditions.
2-Chloro-6-fluoronicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-chloro and para-fluoro substituents provide complementary reactivity for palladium-catalyzed cross-coupling, nucleophilic substitution, and cyclization reactions. The carboxylic acid group facilitates direct derivatization or salt formation, enhancing solubility and purification efficiency. Bench-stable and compatible with standard synthetic workflows, it functions as a key scaffold for developing targeted therapeutics.
|
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: