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 898746-91-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-1H-indole-4-carboxylic acid features a bromine substituent at the 6-position and a carboxylic acid group at the 4-position of the indole core. This configuration enables direct incorporation into bioactive molecule scaffolds, particularly in medicinal chemistry and pharmaceutical development. The electron-deficient nature of the indole ring enhances reactivity in cross-coupling processes, while the carboxylic acid facilitates derivatization via amide or ester formation.
6-Bromo-1H-indole-4-carboxylic acid serves as a versatile building block for the synthesis of indole-based pharmaceuticals and functional materials. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates amide formation, esterification, or direct derivatization. Its stability under standard reaction conditions and compatibility with common protecting groups make it well-suited for multi-step synthetic sequences in medicinal chemistry and process development.
|
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: