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 90923-75-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Methyl-1H-indole-5-carbaldehyde features a conjugated aldehyde group fused to a methyl-substituted indole core, enabling direct incorporation into heterocyclic scaffolds. The electron-rich indole ring facilitates electrophilic functionalization, while the aldehyde serves as a reactive handle for reductive amination or nucleophilic addition under standard conditions. This compound demonstrates robust stability and compatibility with diverse synthetic transformations in medicinal chemistry workflows.
1-Methyl-1H-indole-5-carbaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to functionalized indole scaffolds. Its aldehyde group facilitates standard transformations including reductive amination, Wittig reactions, and nucleophilic additions, while the methyl-substituted indole core provides enhanced stability and compatibility with diverse reaction conditions. The compound exhibits excellent bench stability and is readily purified by column chromatography, making it well-suited for high-throughput synthesis and scale-up applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: