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 58819-88-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-2-methoxynicotinaldehyde features a bromine substituent at the 6-position and a methoxy group at the 2-position on a nicotinaldehyde scaffold. This electron-deficient aldehyde integrates readily into cross-coupling reactions, offering enhanced reactivity in synthetic sequences requiring halogen-functionalized heteroaromatics.
6-Bromo-2-methoxynicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling direct incorporation of bromo and methoxy-functionalized pyridine scaffolds into target molecules. Its aldehyde functionality facilitates efficient coupling reactions, including reductive amination and Wittig transformations, while the bromine atom supports palladium-catalyzed cross-coupling protocols such as Suzuki-Miyaura and Stille reactions. The compound exhibits good bench stability and is readily purified by flash chromatography, making it well-suited for iterative synthesis campaigns and API precursor development.
|
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: