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 181434-76-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Amino-4-chloro-5-methoxybenzoic acid features a strategically positioned amino group and electron-withdrawing chlorine, enabling selective coupling reactions. The methoxy substituent enhances solubility and modulates electronic properties. This scaffold serves as a key building block in the synthesis of bioactive molecules, particularly in medicinal chemistry applications requiring balanced polarity and reactivity.
2-Amino-4-chloro-5-methoxybenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds. Its well-defined functional group set—amino, chloro, methoxy, and carboxylic acid—supports diverse transformations including amide coupling, electrophilic substitution, and Suzuki-Miyaura cross-coupling. The compound exhibits good bench stability and facilitates straightforward purification, making it suitable for both exploratory and process-scale applications.
|
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-P271-P280-P302+P352-P304+P340-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: