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 2313230-37-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 5-amino-4-iodo-2-((methylsulfonyl)methyl)benzoate features a strategically positioned methylsulfonyl group that enhances solubility and metabolic stability, while the iodine and amino functionalities enable efficient cross-coupling reactions. This compound serves as a versatile intermediate in the synthesis of bioactive molecules and functionalized aromatic scaffolds under standard conditions.
Methyl 5-amino-4-iodo-2-((methylsulfonyl)methyl)benzoate serves as a versatile building block for the synthesis of substituted benzimidazoles and other heterocyclic scaffolds via Pd-catalyzed cross-coupling reactions. The iodide group enables efficient Suzuki, Stille, or Sonogashira coupling, while the amino and methylsulfonylmethyl functionalities offer orthogonal reactivity for sequential transformations. Bench-stable and readily purified by flash chromatography, it facilitates streamlined access to complex aromatic architectures in medicinal chemistry and process development 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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: