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 163083-65-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 6-methyl-1H-indole-3-carboxylate features a sterically hindered indole core with a methyl group at the 6-position, enhancing stability and modulating electronic properties. The ester functionality enables direct use in cross-coupling reactions or hydrolysis to the carboxylic acid. This compound serves as a key intermediate in bioactive molecule synthesis, particularly in pharmaceutical and agrochemical scaffolds.
Methyl 6-methyl-1H-indole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, offering a robust indole scaffold with orthogonal functional handles. The methyl ester enables straightforward derivatization via hydrolysis or nucleophilic substitution, while the 6-methyl group provides steric and electronic modulation. This compound exhibits excellent bench stability and facilitates efficient coupling reactions, making it well-suited for medicinal chemistry campaigns and API intermediate development.
|
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: