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 57507-34-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Chloro-4-nitrobenzaldehyde features a chlorine atom at the meta position and a nitro group at the para position relative to the aldehyde, creating a strongly electron-deficient aromatic ring. This configuration enhances reactivity in nucleophilic addition and coupling processes, making it a valuable building block for pharmaceutical intermediates and functional materials.
3-Chloro-4-nitrobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized aromatic systems. Its complementary electron-withdrawing nitro and chloro groups enhance electrophilicity at the aldehyde center, facilitating nucleophilic addition, condensation, and transition-metal-catalyzed coupling reactions. The molecule exhibits good bench stability and is amenable to purification via recrystallization or chromatography, supporting reliable use in medicinal chemistry campaigns and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H317
|
|
|
Precautionary Statements : P261-P272-P280-P302+P352-P333+P317-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: