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 39652-34-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bench-stable, moisture-tolerant carboxylic acid features a methyl group flanked by two chlorine atoms at the 3 and 5 positions, creating a strongly electron-deficient aromatic ring. The para-chloro substitution pattern enhances reactivity in coupling reactions, while the methyl group provides steric and electronic modulation. This structure facilitates efficient derivatization for pharmaceutical intermediates and agrochemical synthesis under standard conditions.
3,5-Dichloro-4-methylbenzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, offering predictable reactivity in esterification, amide coupling, and Suzuki-Miyaura cross-coupling reactions. Its ortho-chloro substitution pattern enhances electrophilic functionalization potential, while the methyl group provides steric and electronic modulation. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring halogen-directed derivatization or incorporation into bioactive heterocyclic scaffolds.
|
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: