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 84459-33-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-4-chlorobenzaldehyde features a dual-halogenated aromatic ring flanked by an aldehyde group, enabling direct functionalization in cross-coupling and electrophilic substitution reactions. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and advanced materials, offering high reactivity under standard conditions.
2-Bromo-4-chlorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The aldehyde functionality facilitates downstream transformations such as reductive amination and Wittig olefination, while the bromo and chloro substituents offer complementary sites for selective functionalization. Bench-stable and compatible with standard purification protocols, it functions effectively in multi-step syntheses requiring precise regiocontrol.
|
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: