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 351458-21-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-4-methyl-3-pyridinol features a bromine substituent at the 5-position and a methyl group at the 4-position on a pyridinol scaffold, enabling selective functionalization in heterocyclic synthesis. The phenolic hydroxyl enhances reactivity for coupling reactions, while the electron-deficient ring facilitates transition metal-catalyzed transformations. This bench-stable compound serves as a key intermediate in medicinal chemistry and agrochemical development.
5-Bromo-4-methyl-3-pyridinol serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The pyridinol core provides a stable, bench-accessible platform for further functionalization, with the methyl group offering mild directing effects. Its compatibility with standard reaction conditions facilitates integration into complex molecular architectures relevant to medicinal chemistry and agrochemical development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: