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 1261685-26-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Chloro-4-cyanobenzoic acid features a conjugated aromatic core bearing orthogonal electron-withdrawing groups: a chloro substituent at the 3-position and a cyano group at the 4-position, flanking a carboxylic acid handle. This arrangement imparts enhanced electrophilicity and solubility in polar aprotic solvents, enabling direct functionalization in cross-coupling and amide coupling reactions under standard conditions.
3-Chloro-4-cyanobenzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles via cyclization or coupling reactions. Its orthogonal functional groups—carboxylic acid, chloro, and nitrile—facilitate diverse transformations including Suzuki-Miyaura coupling, nucleophilic aromatic substitution, and amide formation. The compound exhibits good bench stability and is readily purified by recrystallization, supporting scalable synthesis workflows.
|
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: