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 21296-93-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Chloro-2,3-dimethyl-1H-indole is a halogenated indole derivative featuring a chloro substituent at the 5-position and methyl groups at the 2- and 3-positions. This electron-deficient scaffold integrates readily into bioactive molecule design, offering enhanced metabolic stability and favorable lipophilic character for medicinal chemistry applications.
5-Chloro-2,3-dimethyl-1H-indole serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted indole scaffolds via standard coupling reactions. Its defined substitution pattern offers predictable reactivity in Pd-catalyzed cross-couplings and electrophilic functionalization, while the methyl groups enhance metabolic stability and modulate lipophilicity. Bench-stable and readily purified by column chromatography, it facilitates reproducible synthesis of complex heterocycles and API intermediates.
|
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: