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 2161-96-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-3-nitrothiophene features a thiophene core bearing bromine at the 2-position and a nitro group at the 3-position, creating a highly functionalized heterocycle. This combination enables direct coupling in cross-coupling reactions and facilitates further derivatization through nucleophilic substitution or metal-catalyzed transformations. The electron-deficient nature of the ring enhances reactivity in transition metal-mediated processes.
2-Bromo-3-nitrothiophene serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The nitro group enhances electrophilicity at the adjacent carbon, facilitating sequential functionalization. Its bench-stable crystalline form and compatibility with standard reaction conditions make it well-suited for iterative synthesis of complex thiophene-based scaffolds in medicinal chemistry and materials science.
|
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: