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 244104-55-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(4-Chloro-2-iodophenyl)methanol features a benzene ring bearing chlorine and iodine substituents at the 4- and 2-positions, respectively, with a reactive benzylic alcohol group. This configuration enables direct functionalization in cross-coupling reactions and serves as a key intermediate in pharmaceutical synthesis. The molecule exhibits favorable stability under standard bench conditions and facilitates selective derivatization through its alcohol moiety.
(4-Chloro-2-iodophenyl)methanol serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient access to biaryl and heteroaryl architectures. Its iodide group facilitates reliable Suzuki, Stille, or Negishi coupling under standard conditions, while the chloro substituent offers orthogonal reactivity for sequential functionalization. The benzylic alcohol moiety provides a handle for derivatization, including oxidation to aldehydes or esterification, and contributes to solubility and purification advantages in synthetic 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: