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 1114809-02-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-3-chloro-2-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 imine formation, peptide coupling, and heterocycle synthesis under standard conditions. This electron-deficient aryl aldehyde exhibits enhanced stability and compatibility with diverse reaction media.
6-Bromo-3-chloro-2-fluorobenzaldehyde serves as a versatile building block for the synthesis of substituted heterocycles and pharmaceutical intermediates. Its orthogonal halogenation pattern enables selective cross-coupling reactions, while the aldehyde functionality facilitates efficient derivatization via condensation or reduction. Bench-stable and compatible with standard transition-metal-catalyzed transformations, it functions effectively in multistep 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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: