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 5118-13-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromobenzothiophene serves as a key building block in the synthesis of functionalized heterocycles for pharmaceutical and materials applications. This bench-stable, moisture-tolerant compound features a bromine substituent at the para position, enabling efficient cross-coupling reactions. The fused thiophene ring imparts electron-rich character, enhancing reactivity in palladium-catalyzed transformations.
4-Bromobenzothiophene serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions such as Suzuki, Stille, and Negishi transformations. Its stability under standard reaction conditions, combined with excellent functional group tolerance, makes it ideal for constructing biaryl architectures and heterocyclic scaffolds relevant to pharmaceutical and materials research.
|
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: