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 7099-87-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This oxoacetic acid derivative features a brominated phenyl group at the alpha position, enabling direct integration into cross-coupling and condensation reactions. The electron-withdrawing carbonyl and halogen substituents enhance reactivity in synthetic transformations, while the bench-stable structure supports reliable handling under standard conditions.
2-(4-Bromophenyl)-2-oxoacetic acid serves as a versatile building block for the synthesis of pharmaceutically relevant heterocycles and functionalized aryl ketones. Its brominated aromatic ring enables efficient cross-coupling reactions, while the α-ketoacid functionality facilitates condensation, cyclization, and derivatization under standard organic transformation conditions. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it suitable for iterative synthetic sequences in 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-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: