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 104116-17-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate moiety integrates readily into Suzuki-Miyaura couplings, delivering functionalized naphthalene scaffolds with high efficiency. The methoxy group enhances solubility and stabilizes the boronic acid under standard conditions, enabling straightforward handling and compatibility with diverse reaction partners in synthetic workflows.
(2-Methoxynaphthalen-1-yl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. Its naphthalene core provides enhanced planarity and electronic modulation, while the methoxy group offers predictable regioselectivity and improved solubility. The boronic acid functionality enables efficient coupling with aryl halides and triflates under standard catalytic conditions, facilitating the construction of biaryl architectures common in pharmaceutical and materials chemistry.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
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: