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 25676-75-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-1-methyl-1H-imidazole features a bromine substituent at the 4-position and a methyl group on the imidazole nitrogen, delivering enhanced reactivity in cross-coupling transformations. This bench-stable heterocycle integrates readily into pharmaceutical scaffolds and serves as a key building block in medicinal chemistry.
4-Bromo-1-methyl-1H-imidazole serves as a versatile building block in medicinal chemistry and catalytic synthesis. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the N-methylated imidazole core provides enhanced stability and solubility. The compound functions effectively in Suzuki-Miyaura and Buchwald-Hartwig couplings, offering predictable reactivity and straightforward purification. This makes it a reliable scaffold for constructing functionalized heterocycles in API development and materials science 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: