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 1779-11-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Bromo-3-hydroxy-2-naphthoic acid features a bromine substituent at the 7-position and a hydroxyl group at the 3-position, both strategically positioned on a naphthalene core. This electron-deficient scaffold integrates readily into cross-coupling workflows and offers enhanced solubility in polar media. The carboxylic acid functionality enables direct derivatization for bioconjugation or polymer synthesis.
7-Bromo-3-hydroxy-2-naphthoic acid serves as a versatile building block for naphthoic acid derivatives, enabling efficient functionalization in medicinal chemistry and materials synthesis. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid and phenolic hydroxyl functionalities offer orthogonal handles for derivatization. Its bench-stable solid form and compatibility with standard protection/deprotection protocols support reliable use in multi-step syntheses.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: