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 860435-38-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromo-4-iodoaniline features a dual halogenated aromatic scaffold with bromine at the meta position and iodine at the para position relative to the amino group. This electron-deficient aniline derivative enables direct coupling in cross-coupling reactions, offering site-specific functionalization in pharmaceutical and agrochemical synthesis. The molecule exhibits enhanced stability under standard bench conditions.
3-Bromo-4-iodoaniline serves as a versatile diaryl building block for cross-coupling reactions, enabling efficient access to biaryl scaffolds under Pd-catalyzed conditions. The ortho-bromo and meta-iodo substituents offer complementary reactivity for sequential functionalization, with excellent bench stability and straightforward purification. Its dual halogenation pattern facilitates modular synthesis of complex heterocycles and pharmaceutical intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H315-H319-H332-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: