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 17570-26-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(E)-3-(3-Methoxyphenyl)acrylic acid features a conjugated system with a para-methoxy-substituted phenyl ring, enhancing electron delocalization and stability. This bench-stable enone scaffold integrates readily into synthetic routes for bioactive compounds, offering predictable reactivity in coupling and cyclization processes under standard conditions.
(E)-3-(3-Methoxyphenyl)acrylic acid serves as a versatile building block for synthesizing conjugated systems and bioactive heterocycles. Its well-defined geometry and stability enable reliable use in Michael additions, Diels–Alder reactions, and transition-metal-catalyzed couplings. The methoxy group enhances solubility and provides a handle for further functionalization, while the carboxylic acid facilitates direct derivatization or salt formation. This compound is particularly valuable for medicinal chemistry campaigns targeting kinase inhibitors and anti-inflammatory agents.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: