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 627526-50-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate ester integrates a sterically shielded tetramethylcyclopentadienyl core with a 4-methylnaphthalen-1-yl group, enabling stable coupling in Suzuki-Miyaura reactions. The electron-rich naphthyl moiety enhances reactivity while the bulky methyl substituents confer moisture tolerance and bench stability under standard conditions.
4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its naphthyl moiety enables efficient construction of biaryl scaffolds with enhanced solubility and thermal stability. The tetramethyl-substituted dioxaborolane ring ensures high functional group tolerance and minimal protodeboronation, facilitating reliable coupling under standard conditions. This reagent functions effectively in late-stage diversification and heterocyclic synthesis workflows.
|
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: