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 1006715-27-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-3-iodobenzonitrile features a dual halogenated aromatic core with complementary reactivity at bromine and iodine sites. This orthogonal functionality enables selective cross-coupling transformations in late-stage diversification. The nitrile group enhances solubility and provides a handle for further functionalization, making this compound valuable in the synthesis of complex pharmaceutical intermediates and advanced materials.
4-Bromo-3-iodobenzonitrile serves as a versatile diaryl building block for cross-coupling reactions, enabling the synthesis of biaryl and heteroaryl scaffolds under palladium-catalyzed conditions. The bromo and iodo substituents offer orthogonal reactivity, facilitating sequential functionalization. The nitrile group provides a handle for downstream transformations, including hydrolysis to carboxylic acids or reduction to aldehydes. Bench-stable and readily purified by crystallization, it supports scalable synthesis in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H303-H313-H333
|
|
|
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: