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 90948-03-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Bromo-2-iodonaphthalene features a naphthalene core with adjacent bromo and iodo substituents, enabling sequential cross-coupling reactions. This dual-halogenated scaffold supports precise functionalization in late-stage diversification, particularly in palladium-catalyzed coupling sequences. The ortho-halo arrangement facilitates controlled reactivity, where one halogen selectively engages under mild conditions while the other remains intact. This enables efficient access to complex biaryl architectures with tailored substitution patterns.
1-Bromo-2-iodonaphthalene serves as a versatile biaryl building block in transition-metal-catalyzed cross-coupling reactions. The orthogonal reactivity of bromo and iodo groups enables sequential functionalization, facilitating the construction of complex naphthalene-based scaffolds. Its bench-stable nature and compatibility with palladium-catalyzed coupling protocols make it well-suited for iterative 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 : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: