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 487-68-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Mesitaldehyde features a sterically hindered trimethyl-substituted aromatic ring that imparts exceptional stability and resistance to oxidation. This electron-rich aldehyde integrates readily into condensation reactions, enabling efficient access to complex heterocyclic scaffolds under mild conditions.
Mesitaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted aromatic systems and heterocycles. Its three methyl groups confer enhanced stability and facilitate electrophilic substitution reactions, while the aldehyde functionality allows for straightforward transformations including imine formation, aldol condensations, and reductive amination. The compound's bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07,GHS09
|
|
Signal Word : Warning
|
UN#: 3082
|
|
Class : 9
|
Packing Group : Ⅲ
|
|
Hazard Statements : H315-H351-H411
|
|
|
Precautionary Statements : P264-P273-P280-P302+P352-P362-P391-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: