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 170489-16-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1,4-Dimethyl-1H-indole-3-carbaldehyde features a benzene-fused indole core with strategically positioned methyl groups enhancing solubility and steric profile. The aldehyde functionality enables direct coupling in C–C bond-forming reactions. This scaffold integrates readily into bioactive molecule design, offering improved metabolic stability compared to unsubstituted analogs.
1,4-Dimethyl-1H-indole-3-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The aldehyde functionality enables efficient coupling reactions, while the methylated indole core provides enhanced stability and favorable electronic properties. It functions effectively in reductive amination, Wittig, and Suzuki-type transformations, offering reliable access to substituted indole scaffolds commonly found in bioactive molecules. Its bench-stable nature and straightforward purification support scalable applications in drug discovery 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: