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 589-10-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(2-Bromoethoxy)benzene features a brominated ethoxy chain attached to a benzene ring, enabling direct functionalization in cross-coupling reactions. This aryl bromide serves as a robust electrophilic handle for palladium-catalyzed transformations, offering high reactivity under standard conditions. The molecule exhibits excellent stability and compatibility with diverse reaction environments.
(2-Bromoethoxy)benzene serves as a versatile building block in synthetic organic chemistry, enabling efficient C–O bond formation via palladium-catalyzed coupling reactions. Its bromine substituent facilitates reliable cross-coupling with boronic acids and nucleophiles under standard conditions, while the ether linkage offers stability and compatibility with diverse functional groups. This compound functions effectively in the construction of aryl ether scaffolds common in pharmaceutical intermediates and agrochemicals.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: