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 16650-63-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 3-bromo-1-naphthoate is a brominated naphthoate ester featuring a reactive halogen at the 3-position of the naphthalene core. This electrophilic site enables direct functionalization in cross-coupling reactions, particularly Suzuki-Miyaura and Stille processes. The methyl ester group provides synthetic versatility for further derivatization. Bench-stable and moisture-tolerant under standard conditions, it integrates seamlessly into complex molecule assembly workflows.
Methyl 3-bromo-1-naphthoate serves as a versatile building block for the synthesis of naphthalene-based pharmaceutical intermediates and functional materials. The bromine at the 3-position enables palladium-catalyzed cross-coupling reactions, while the ester group offers compatibility with standard transformations such as hydrolysis, reduction, or nucleophilic substitution. Its bench-stable nature and predictable reactivity facilitate efficient integration into multi-step synthetic sequences.
|
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: