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 22223-49-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This methyl ester derivative of 2-amino-3-methylbenzoic acid features a strategically positioned amino group flanked by a methyl-substituted aromatic ring and a labile ester moiety. The electron-donating amino group enhances reactivity in electrophilic substitution, while the methyl group imparts steric stabilization. This combination enables efficient incorporation into peptide mimetics and heterocyclic scaffolds under standard conditions.
2-Amino-3-methylbenzoic acid methyl ester serves as a versatile building block in medicinal chemistry, enabling direct access to substituted benzimidazoles and other heterocyclic scaffolds via cyclization reactions. The ortho-amino and ester functionalities offer complementary reactivity for sequential transformations, while the methyl group provides steric and electronic tuning. Bench-stable and readily purified by column chromatography, it functions effectively in standard coupling and cyclization protocols.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: