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 182234-10-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Methyl-1H-indol-4-amine features a methyl-substituted indole core with a primary amine at the 4-position, delivering enhanced solubility and reactivity in synthetic transformations. This electron-rich scaffold integrates readily into bioactive molecule frameworks, particularly in kinase inhibitors and fluorescent probes. The pendant amine enables direct coupling reactions under mild conditions, streamlining access to functionalized heterocycles.
2-Methyl-1H-indol-4-amine serves as a versatile building block in medicinal chemistry, enabling direct incorporation into diverse heterocyclic scaffolds. Its ortho-methylated indole core exhibits enhanced metabolic stability and facilitates regioselective functionalization at the C4 position. The primary amine group enables straightforward derivatization via amidation, alkylation, or coupling reactions, supporting rapid library synthesis. Bench-stable and readily purified by standard chromatographic methods, it functions effectively in both small-molecule discovery and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: