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 474330-54-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 5-amino-2-bromo-4-methylbenzoate features a brominated aromatic core with complementary amino and methyl substituents, enabling selective coupling in cross-coupling reactions. The electron-donating amino group enhances reactivity at the para-position, while the ester functionality offers straightforward derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and functionalized pharmaceuticals under standard conditions.
Methyl 5-amino-2-bromo-4-methylbenzoate serves as a versatile building block in medicinal chemistry, enabling selective functionalization at the amino and bromo sites. The ortho-bromo group facilitates palladium-catalyzed cross-coupling reactions, while the amino function supports acylation, sulfonation, or diazotization. Bench-stable and amenable to purification by recrystallization, it functions effectively in the synthesis of substituted heterocycles and bioactive scaffolds.
|
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: