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 56961-76-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3,4,5-Trichlorobenzaldehyde features a highly electron-deficient aromatic ring stabilized by three chlorine substituents, enabling robust coupling reactions. This bench-stable aldehyde integrates efficiently into synthetic sequences requiring halogenated electrophiles and serves as a key intermediate in the development of functionalized pharmaceuticals and agrochemicals.
3,4,5-Trichlorobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of substituted heterocycles and pharmaceutical intermediates. Its electron-deficient aromatic ring enhances reactivity in nucleophilic addition and condensation reactions, while the aldehyde functionality offers straightforward derivatization via imine formation or reduction. Bench-stable and readily purified by crystallization, it functions efficiently in standard workflows requiring high functional group tolerance and predictable regioselectivity.
|
GHS Pictogram :
|
GHS No : GHS07,GHS05
|
|
Signal Word : Danger
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H314-H335
|
|
|
Precautionary Statements : P260-P264-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P363-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: