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 5769-33-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-2,6-dimethylbenzaldehyde features a sterically hindered aromatic core with electron-withdrawing bromine and electron-donating methyl groups, enabling selective functionalization. The aldehyde moiety facilitates efficient coupling reactions, while the ortho-methyl substitution enhances stability under standard conditions. This compound serves as a key building block in synthesizing bioactive molecules and advanced materials.
4-Bromo-2,6-dimethylbenzaldehyde serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering enhanced steric shielding and electronic modulation via its ortho-methyl groups. The aldehyde functionality enables reliable transformations in reductive amination, Wittig reactions, and coupling processes, while the bromine substituent facilitates subsequent cross-coupling reactions such as Suzuki or Stille couplings. Bench-stable and readily purified by recrystallization, it functions as a versatile scaffold for constructing complex aromatic systems with controlled regiochemistry.
|
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: