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 1071224-34-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Bromobenzo[c][1,2,5]thiadiazole-4-carbaldehyde features a brominated heterocyclic core fused with a thiadiazole ring and a formyl group at the 4-position. This electron-deficient scaffold integrates readily into conjugated systems, enabling efficient coupling in transition-metal-catalyzed transformations. The molecule exhibits bench-stable handling characteristics and tolerates a range of reaction conditions, making it suitable for synthesizing advanced materials and functionalized aromatic intermediates.
7-Bromobenzo[c][1,2,5]thiadiazole-4-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromo and aldehyde functionalities. The aldehyde group facilitates condensation and derivatization under mild conditions, while the thiadiazole core provides enhanced electronic properties and metabolic stability. Bench-stable and compatible with common protecting groups, it functions effectively in the construction of bioactive scaffolds and functional materials.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: