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 137088-51-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-tert-Butyl 2,3-dihydroindole-1,2-dicarboxylate serves as a robust, bench-stable scaffold for indole-based synthesis. The protected dihydroindole core facilitates direct functionalization at C2 and C3 positions, enabling efficient access to complex heterocycles. This dicarboxylate moiety enhances solubility in organic media while maintaining compatibility with standard coupling and cyclization protocols.
1-tert-Butyl 2,3-dihydroindole-1,2-dicarboxylate serves as a versatile scaffold for the synthesis of indole-based heterocycles and bioactive molecules. Its dihydroindole core enables direct functionalization at C2 and C3 positions, while the tert-butyl ester groups offer orthogonal protection and facile deprotection under mild acidic conditions. The compound exhibits excellent bench stability and compatibility with standard coupling reactions, facilitating efficient access to complex molecular architectures in medicinal chemistry and process development workflows.
|
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: