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 53855-47-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-methyl-1H-indole-3-carboxylate features a sterically hindered indole core with a strategically positioned ester group, enabling direct functionalization at the C3 position. This bench-stable scaffold integrates readily into synthetic sequences for pharmaceutical and agrochemical intermediates, offering high compatibility in cross-coupling and electrophilic substitution reactions.
Ethyl 2-methyl-1H-indole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted indole scaffolds. Its ethyl ester functionality facilitates subsequent transformations such as hydrolysis, reduction, and coupling reactions, while the 2-methyl group enhances stability and directs electrophilic substitution. This compound exhibits excellent bench stability and compatibility with standard synthetic workflows, making it well-suited for medicinal chemistry and process development applications.
|
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: