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 3705-21-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Hydroxy-1H-indole-3-carboxylic acid features a fused indole core with strategically positioned hydroxyl and carboxylic acid groups, enabling direct integration into bioactive molecule scaffolds. The electron-rich indole system supports diverse functionalization, while the polar substituents enhance solubility and facilitate conjugation in synthetic pathways. This compound serves as a key building block for pharmaceutical intermediates and probe development.
5-Hydroxy-1H-indole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct access to substituted indole scaffolds through standard functional group manipulations. Its hydroxyl and carboxylic acid groups offer orthogonal reactivity for derivatization, including amidation, esterification, and metal-catalyzed coupling reactions. The molecule exhibits good bench stability and facilitates purification via recrystallization or flash chromatography, supporting reliable integration into multi-step syntheses of bioactive compounds.
|
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: