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 31819-37-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromo-2,5-dimethylthiophene is a bench-stable, electron-rich heterocycle featuring a bromine substituent at the 3-position and methyl groups flanking the sulfur atom. This configuration enables direct coupling in cross-coupling reactions, facilitating rapid access to functionalized thiophene architectures for organic electronics and synthetic intermediates.
3-Bromo-2,5-dimethylthiophene serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent and electron-rich thiophene core. The methyl groups enhance solubility and facilitate functionalization at adjacent positions. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H227-H302-H315-H319-H335
|
|
|
Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: