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 24297-59-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(1H-Indol-1-yl)acetic acid features a bioactive indole core linked to a carboxylic acid side chain, enabling direct integration into peptide conjugates and small-molecule libraries. This scaffold supports rapid derivatization for probing receptor-ligand interactions in neurochemical and oncology research.
2-(1H-Indol-1-yl)acetic acid serves as a versatile building block for indole-based bioactive molecules, enabling straightforward incorporation into pharmaceutical and agrochemical scaffolds. Its carboxylic acid functionality facilitates direct amidation, esterification, or coupling reactions under standard conditions. The molecule exhibits bench stability and tolerates diverse functional groups, making it well-suited for medicinal chemistry campaigns requiring efficient access to indole-containing compounds.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H318
|
|
|
Precautionary Statements : P264-P270-P280-P305+P351+P338-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: