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 95470-42-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-bromo-4-methyl-1H-imidazole-5-carboxylate is a bench-stable, moisture-tolerant heterocyclic building block featuring a brominated imidazole core and an ester-functionalized C5 position. This compound integrates readily into cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive imidazole derivatives.
Ethyl 2-bromo-4-methyl-1H-imidazole-5-carboxylate serves as a versatile building block for the synthesis of imidazole-based heterocycles, enabling palladium-catalyzed cross-coupling reactions and nucleophilic substitution processes. The bromo group facilitates C–C and C–N bond formation under mild conditions, while the ester functionality supports further derivatization. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for medicinal chemistry campaigns and process development.
|
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: