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 942473-86-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-3-fluorothiophenol features a thiophenol scaffold with complementary halogen substituents at the 4- and 3-positions, enabling selective cross-coupling and functionalization. The electron-deficient aromatic ring enhances reactivity in palladium-catalyzed transformations, while the thiol group provides a robust anchor for conjugation. This bifunctional architecture supports efficient integration into complex molecular frameworks under standard conditions.
4-Bromo-3-fluorothiophenol serves as a valuable building block for the synthesis of functionalized thiophene derivatives. Its orthogonal halogen substituents enable selective cross-coupling reactions, while the thiol group facilitates direct conjugation or derivatization. The molecule exhibits bench stability and compatibility with standard purification methods, making it well-suited for applications in medicinal chemistry and materials science workflows.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 1759
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H314
|
|
|
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: