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 39689-58-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This indole-acetic acid derivative features a strategically positioned carboxylic acid group on the side chain, enabling direct conjugation or derivatization. The aromatic indolyl moiety imparts enhanced solubility and stability in aqueous systems, facilitating use in bioconjugation workflows and peptide modifications.
2-(1H-Indol-6-yl)acetic acid serves as a versatile building block for the synthesis of indole-based bioactive molecules, enabling efficient conjugation via carboxylic acid functionalization. Its stability under standard reaction conditions and compatibility with common coupling protocols facilitate straightforward derivatization for medicinal chemistry applications. The molecule functions as a key scaffold in the development of heterocyclic compounds and pharmaceutical intermediates requiring direct indole substitution at the 6-position.
|
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: