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 350-46-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Fluoro-4-nitrobenzene features a para-substituted aromatic ring with complementary electron-withdrawing nitro and fluorine groups, enabling efficient nucleophilic aromatic substitution under mild conditions. This bench-stable compound integrates readily into synthetic sequences requiring selective C–X bond activation, particularly in the construction of bioactive heterocycles and functionalized aryl building blocks.
1-Fluoro-4-nitrobenzene serves as a versatile arylating agent in nucleophilic aromatic substitution reactions, enabling efficient construction of biaryl and heterocyclic scaffolds. Its ortho-directing nitro group enhances reactivity while maintaining bench stability and compatibility with diverse nucleophiles, including amines, thiols, and carbanions. The compound functions reliably in standard synthetic workflows, facilitating the introduction of complex functional groups under mild conditions.
|
GHS Pictogram :
|
GHS No : GHS06,GHS08
|
|
Signal Word : Danger
|
UN#: 2810
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H227-H302+H312-H331-H373-H412
|
|
|
Precautionary Statements : P210-P260-P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P362+P364-P370+P378-P403-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: