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 7745-92-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Iodo-1-methyl-4-nitrobenzene features a sterically accessible iodine atom paired with a para-nitro group, enabling efficient cross-coupling reactions under mild conditions. The methyl substitution enhances solubility and stability in organic solvents, while the electron-deficient aryl ring facilitates palladium-catalyzed transformations. This compound serves as a key building block for functionalized arenes in medicinal chemistry and materials science.
2-Iodo-1-methyl-4-nitrobenzene serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki, Stille, and Negishi reactions due to its well-defined reactivity profile. The iodine moiety facilitates reliable coupling under mild conditions, while the methyl and nitro groups provide orthogonal functionalization sites. This compound exhibits excellent bench stability and is readily purified by recrystallization, making it ideal for iterative synthesis of complex aromatic scaffolds and functionalized heterocycles in medicinal and process chemistry workflows.
|
GHS Pictogram :
|
GHS No : GHS07,GHS09
|
|
Signal Word : Warning
|
UN#: 3077
|
|
Class : 9
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H312-H332-H401-H411
|
|
|
Precautionary Statements : P261-P264-P270-P271-P273-P280-P363-P391-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: