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 30478-88-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Bromonaphthalen-2-ol features a bromine substituent at the 3-position and a phenolic hydroxyl group at the 2-position of the naphthalene core. This combination enables direct functionalization in cross-coupling reactions while maintaining solubility under standard conditions. The electron-rich aromatic system facilitates efficient transition metal catalysis, making this compound valuable for synthesizing complex polycyclic architectures.
3-Bromonaphthalen-2-ol serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromine substituent and phenolic functionality. The ortho-hydroxyl group enhances regioselectivity in subsequent transformations and facilitates metal coordination, while the naphthalene core provides robust aromatic stability. This compound exhibits excellent bench stability and is readily purified by recrystallization or column chromatography, making it ideal for use in the construction of complex heterocycles, pharmaceutical intermediates, and functional materials.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 1759
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H315-H318-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: