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 99329-85-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-4-fluoro-5-nitrobenzaldehyde features a trifunctional aromatic core bearing chlorine, fluorine, and nitro groups ortho to the aldehyde, enabling strategic integration into complex molecular architectures. The electron-deficient ring enhances reactivity in nucleophilic substitution and coupling processes, while the aldehyde functionality provides a handle for imine formation or derivatization under mild conditions. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and functional materials.
2-Chloro-4-fluoro-5-nitrobenzaldehyde serves as a versatile electrophilic building block in the synthesis of advanced heterocycles and pharmaceutical intermediates. Its orthogonal halogen (Cl, F) and nitro groups enable selective functionalization via cross-coupling or reduction sequences, while the aldehyde functionality facilitates condensation reactions. Bench-stable and compatible with standard purification methods, it supports scalable access to complex scaffolds in medicinal chemistry and materials science applications.
|
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: