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 1182709-86-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Dichloro-4-fluorobenzaldehyde features a trifluorinated aromatic core with strategically positioned halogens enabling direct functionalization in cross-coupling and electrophilic substitution reactions. The aldehyde group provides a reactive handle for reductive amination, Schiff base formation, and incorporation into bioactive scaffolds. This electron-deficient benzaldehyde exhibits enhanced stability under standard conditions and facilitates efficient derivatization in synthetic medicinal chemistry workflows.
2,6-Dichloro-4-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted aromatic scaffolds. Its orthogonal halogenation pattern facilitates selective cross-coupling reactions, while the aldehyde group supports imine formation, reductive amination, and condensation protocols. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring high functional group tolerance and predictable reactivity.
|
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: