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 110046-60-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2,2'-bithiophene-5'-carboxaldehyde features a brominated bithiophene core with a terminal aldehyde group, enabling direct coupling in cross-coupling reactions. The electron-deficient aldehyde facilitates conjugation and functionalization, while the bromine atom serves as a handle for palladium-catalyzed transformations. This compound integrates readily into π-conjugated systems for organic electronics and synthetic intermediates.
5-Bromo-2,2'-bithiophene-5'-carboxaldehyde serves as a versatile building block for conjugated materials and heterocyclic synthesis. The aldehyde functionality enables direct coupling in Ullmann-type reactions and Suzuki-Miyaura protocols, while the bromo group offers orthogonal reactivity for palladium-catalyzed cross-couplings. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthetic sequences in organic electronics and medicinal chemistry applications.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: