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 19434-34-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Phenoxybenzaldehyde features a phenoxy-substituted benzaldehyde core, offering enhanced solubility and stability in organic synthesis. The electron-withdrawing aldehyde group pairs with the ortho-phenoxy moiety to enable selective coupling reactions. This compound serves as a key scaffold for pharmaceutical intermediates and functional materials, particularly in ligand design and heterocyclic derivatization under standard conditions.
2-Phenoxybenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biaryl and heterocyclic scaffolds. Its ortho-phenoxy substituent enhances electronic modulation and steric profile, while the aldehyde functionality facilitates reliable imine formation, reductive amination, and transition-metal-catalyzed coupling reactions. The compound exhibits excellent bench stability and is compatible with common protecting group strategies, making it well-suited for medicinal chemistry and process development 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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: