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 529-35-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bench-stable phenolic compound features a fused bicyclic structure with a hydroxyl group at the 1-position, enabling direct incorporation into synthetic routes requiring a rigid, electron-rich aromatic scaffold. The tetrahydronaphthalene core offers enhanced solubility and reduced volatility compared to unsubstituted naphthalene derivatives, facilitating handling in multi-step organic transformations.
5,6,7,8-Tetrahydronaphthalen-1-ol serves as a versatile synthetic intermediate featuring a benzylic alcohol within a partially saturated naphthalene framework. Its stability under standard reaction conditions enables reliable functionalization via oxidation, protection, or coupling reactions. The molecule functions as a key building block in the synthesis of bioactive heterocycles and pharmaceutical scaffolds, offering predictable reactivity and compatibility with common protecting group strategies.
|
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: