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 87885-43-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-3-nitropyrazine is a heterocyclic building block featuring a chloro group at the 2-position and a nitro group at the 3-position on the pyrazine ring. This electron-deficient scaffold enables selective cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive molecules, particularly in medicinal chemistry and agrochemical development.
2-Chloro-3-nitropyrazine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloro substituent. The nitro group enhances electrophilicity at the pyrazine ring, facilitating nucleophilic substitution and serving as a handle for downstream reduction to an amine. Its bench-stable crystalline form and compatibility with standard synthetic protocols make it ideal for constructing complex nitrogen-containing scaffolds relevant to medicinal chemistry and agrochemical development.
|
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: