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 18791-79-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromothiophene-3-carbaldehyde features a brominated thiophene ring fused to an aldehyde group, enabling direct functionalization in cross-coupling and condensation reactions. The electron-deficient thiophene core enhances reactivity in palladium-catalyzed transformations, while the aldehyde moiety serves as a versatile handle for further derivatization. This bench-stable compound integrates efficiently into complex molecular architectures under standard conditions.
5-Bromothiophene-3-carbaldehyde serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the thiophene core. Its aldehyde group facilitates nucleophilic additions and condensation reactions, while the bromine substituent supports palladium-catalyzed cross-couplings. The molecule exhibits bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis of heterocyclic scaffolds and advanced intermediates in medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H317-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: