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 2178-24-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl (2-bromophenyl)acetate features a brominated phenyl ring positioned ortho to the acetate ester, enabling direct functionalization in cross-coupling reactions. This bench-stable reagent integrates seamlessly into synthetic sequences requiring aryl halide handles, offering predictable regiochemistry and compatibility with palladium-catalyzed transformations under standard conditions.
Ethyl (2-bromophenyl)acetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenylacetic acid derivatives and functionalized heterocycles. The ortho-bromo substituent facilitates palladium-catalyzed cross-coupling reactions, while the ester group supports selective transformations including reduction, hydrolysis, and nucleophilic substitution. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and process development workflows.
|
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-P302+P352-P304+P340
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: