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 1256955-36-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-amino-4-bromo-5-methoxybenzoate features a strategically positioned bromine atom and methoxy group on the aromatic ring, enabling selective cross-coupling reactions. The amino substituent enhances solubility and reactivity in transition-metal-catalyzed transformations. This bench-stable derivative serves as a key intermediate in synthesizing bioactive heterocycles and functionalized pharmaceutical scaffolds.
Methyl 2-amino-4-bromo-5-methoxybenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, benzoxazoles, and other heterocyclic scaffolds. The molecule’s ortho-amino and bromo functionalities facilitate sequential cross-coupling and cyclization reactions under standard conditions. Bench-stable with excellent functional group tolerance, it simplifies purification and supports scalable transformations in multi-step syntheses.
|
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: