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 1448776-78-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-3-methyl-4-(trifluoromethyl)pyridine features a trifluoromethyl group that enhances electron deficiency and metabolic stability, while the bromo substituent enables palladium-catalyzed cross-coupling reactions. The methyl group provides steric bulk, improving selectivity in synthetic transformations. This pyridine scaffold serves as a key building block in medicinal chemistry for developing kinase inhibitors and bioactive heterocycles.
2-Bromo-3-methyl-4-(trifluoromethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromide and electron-deficient pyridine core. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the methyl substituent provides steric control. This compound exhibits bench stability, facilitates straightforward purification, and functions effectively in Suzuki, Stille, and Negishi coupling protocols for constructing complex heterocyclic scaffolds.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H311-H331
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: