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 14222-98-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde features three electron-deficient aldehyde groups positioned at the 2, 4, and 6 positions of a benzene ring, enabling high reactivity in nucleophilic addition and condensation reactions. The trichloro substitution enhances stability and facilitates selective functionalization under mild conditions. This trialdehyde serves as a rigid, symmetric scaffold for constructing complex molecular architectures in materials science and synthetic organic chemistry.
2,4,6-Trichlorobenzene-1,3,5-tricarbaldehyde serves as a versatile tri-functional building block in synthetic organic chemistry, enabling the construction of complex heterocyclic scaffolds and functionalized aromatic systems. Its three electron-deficient aldehyde groups facilitate efficient condensation reactions, including Mannich and Knoevenagel-type processes, with excellent bench stability and straightforward purification. Functions as a key intermediate in the synthesis of advanced ligands, pharmaceutical precursors, and materials with defined spatial architecture.
|
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: