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 2840-29-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Amino-4-bromobenzoic acid features a bromine atom at the para position relative to the carboxylic acid group, enhancing electrophilic substitution reactivity. The amino functionality provides a versatile handle for coupling reactions, while the carboxylate enables salt formation and conjugation. This dual-functional architecture supports integration into bioconjugates, pharmaceutical intermediates, and functional materials under standard bench conditions.
3-Amino-4-bromobenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles, quinazolines, and other heterocyclic scaffolds. The amino and bromo groups offer orthogonal reactivity for palladium-catalyzed coupling and electrophilic substitution, while the carboxylic acid facilitates amide formation or salt crystallization. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring functional group tolerance and predictable regiochemistry.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: