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 83004-13-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-6-ethylpyridine features a bromine substituent at the 2-position and an ethyl group at the 6-position of the pyridine ring, creating a sterically accessible site for cross-coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and functional materials, offering high reactivity under palladium-catalyzed conditions with minimal side-product formation.
2-Bromo-6-ethylpyridine serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. Its bromine substituent enables reliable Suzuki, Stille, and Negishi couplings, while the pyridine core provides a stable heteroaromatic scaffold with defined electronic properties. The ethyl group enhances solubility and modulates reactivity, offering favorable bench stability and ease of purification in multi-step syntheses.
|
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: