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 103261-68-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 5-cyano-2-methylbenzoate features a conjugated cyano group flanked by electron-rich methyl and ester functionalities, enabling efficient integration into heterocyclic syntheses. This bench-stable derivative serves as a key building block for bioactive molecule scaffolds, offering enhanced solubility and compatibility in transition-metal-catalyzed coupling reactions.
Methyl 5-cyano-2-methylbenzoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted benzoic acid derivatives and heterocyclic scaffolds. Its ortho-methyl and meta-cyano groups provide defined regiochemistry for downstream functionalization, while the ester moiety offers compatibility with standard hydrolysis, reduction, and coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: