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 42860-04-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-3-iodobenzoic acid features a benzene ring bearing strategically positioned chlorine and iodine substituents flanking a carboxylic acid group. This electronic configuration enables direct functionalization in cross-coupling reactions, while the carboxylic acid facilitates conjugation or derivatization. The molecule exhibits robust stability under standard handling conditions.
4-Chloro-3-iodobenzoic acid serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling the construction of biaryl and heteroaryl scaffolds under standard conditions. The ortho-halogenated motif provides predictable reactivity in Suzuki, Stille, and Negishi couplings, while the carboxylic acid group allows for direct derivatization or salt formation to enhance solubility and purification. Bench-stable and readily isolated, it functions effectively in synthetic sequences requiring functional group tolerance and orthogonal reactivity.
|
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: