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 63969-83-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-(2-formylphenyl)acetate features a benzaldehyde moiety fused to an acetic acid ester, enabling direct integration into transition-metal-catalyzed couplings and cycloadditions. The ortho-aldehyde group enhances reactivity in electrophilic transformations, while the methyl ester offers stability under standard conditions. This compound serves as a key building block for heterocyclic scaffolds in medicinal chemistry and materials synthesis.
Methyl 2-(2-formylphenyl)acetate serves as a versatile synthon in heterocyclic synthesis, enabling efficient access to benzimidazole and benzothiazole scaffolds via condensation with diamines or thioureas. The ortho-aldehyde functionality facilitates intramolecular cyclizations, while the ester group offers compatibility with standard functional group manipulations. Its bench-stable nature and straightforward purification make it well-suited for iterative synthetic campaigns in medicinal chemistry and process development.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: