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 2040-86-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-6-iodophenol delivers a dual halogenated aromatic scaffold for precision synthesis, combining bromine and iodine substituents at meta positions to enable selective cross-coupling reactions. This bench-stable phenolic building block facilitates efficient access to complex heterocycles and functionalized aryl systems under standard conditions.
2-Bromo-6-iodophenol serves as a versatile diaryl building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its orthogonal halogen reactivity—bromine typically undergoing Suzuki or Stille coupling while iodine participates in Buchwald-Hartwig amination—facilitates sequential functionalization. The phenolic hydroxyl group offers additional handle for derivatization or protection, enhancing synthetic flexibility. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of complex aromatic architectures relevant to medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 1759
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: