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 339366-85-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Methyl-1H-indole-7-carboxylic acid features a sterically accessible indole core with a carboxylic acid group at the C7 position, enabling direct conjugation in peptide and heterocyclic syntheses. The methyl substitution enhances solubility and metabolic stability, while the electron-deficient aromatic system facilitates electrophilic functionalization under mild conditions. This scaffold serves as a key building block for bioactive molecules in medicinal chemistry.
2-Methyl-1H-indole-7-carboxylic acid serves as a versatile building block for the synthesis of indole-based bioactive molecules. Its carboxylic acid functionality enables direct amidation, esterification, and coupling reactions under standard conditions. The methyl group at the 2-position enhances metabolic stability and modulates electronic properties, while the indole core provides a rigid scaffold suitable for medicinal chemistry applications. Bench-stable and readily purified by recrystallization, it functions effectively in both small-molecule discovery and process-scale synthesis.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: