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 23794-16-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-1-(2-chloro-4-pyridyl)ethanone features a brominated acetyl group attached to a chloropyridyl scaffold, enabling direct integration into cross-coupling and heterocyclic synthesis. The electron-deficient pyridine ring enhances reactivity in nucleophilic substitution, while the bromo functionality provides a handle for palladium-catalyzed transformations. This compound serves as a key intermediate for bioactive molecule development.
2-Bromo-1-(2-chloro-4-pyridyl)ethanone serves as a versatile building block for constructing bioactive heterocycles and pharmaceutical intermediates. Its bromoacetyl functionality enables efficient nucleophilic substitution, while the pyridyl moiety offers orthogonal reactivity and enhanced solubility. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in standard coupling reactions, cyclizations, and late-stage functionalization protocols common in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 3261
|
|
Class : 8
|
Packing Group : Ⅱ
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: