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 189748-25-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 2-(5-bromo-2-nitrophenyl)acetate features a brominated nitroaryl core with a pendant ester group, enabling direct incorporation into cross-coupling and functionalization cascades. The electron-deficient aromatic system enhances reactivity in palladium-mediated transformations, while the methyl ester serves as a handle for subsequent derivatization under mild conditions. This compound exhibits robust stability under standard bench handling protocols.
Methyl 2-(5-bromo-2-nitrophenyl)acetate serves as a versatile building block for the synthesis of substituted heterocycles and bioactive intermediates. The molecule combines a bromo substituent for late-stage functionalization via cross-coupling and a nitro group amenable to reduction, enabling access to anilines or further derivatization. Its methyl ester functionality supports standard transformations including hydrolysis, amidation, and coupling reactions. Bench-stable and readily purified by recrystallization, it facilitates efficient integration into multi-step synthetic sequences common in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H311-H331
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: