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 53484-16-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-1-methyl-1H-1,3-benzodiazole features a brominated benzodiazole core with a methyl group at the 1-position, offering enhanced stability and tailored reactivity. This electron-deficient heterocycle integrates readily into synthetic scaffolds for medicinal chemistry and materials science applications, particularly in cross-coupling transformations and pharmaceutical lead optimization.
6-Bromo-1-methyl-1H-1,3-benzodiazole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the methyl group enhances solubility and stability. The benzodiazole core provides a rigid, planar scaffold with favorable electronic properties for drug discovery applications. This compound exhibits excellent bench stability and facilitates efficient functionalization in standard synthetic 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: