CymitQuimica logo

CAS 207981-49-5

:

2,3,5,6-Tetrafluorophenyl isothiocyanate

Description:
2,3,5,6-Tetrafluorophenyl isothiocyanate is a chemical compound characterized by the presence of a phenyl ring substituted with four fluorine atoms and an isothiocyanate functional group. The fluorine substitutions at the 2, 3, 5, and 6 positions of the phenyl ring significantly influence its reactivity and properties, making it a highly polar and potentially reactive compound. Isothiocyanates are known for their ability to participate in nucleophilic reactions, often serving as electrophiles in organic synthesis. This compound is typically used in the synthesis of various organic molecules, including pharmaceuticals and agrochemicals, due to its unique reactivity profile. Additionally, the presence of fluorine atoms can enhance the compound's stability and lipophilicity, which may affect its biological activity and environmental behavior. As with many isothiocyanates, it is important to handle this compound with care, as it may pose health risks upon exposure. Proper safety protocols should be followed when working with this substance in a laboratory setting.
Formula:C7HF4NS
InChI:InChI=1/C7HF4NS/c8-3-1-4(9)6(11)7(5(3)10)12-2-13/h1H
SMILES:c1c(c(c(c(c1F)F)N=C=S)F)F
Synonyms:
  • 1,2,4,5-Tetrafluoro-3-isothiocyanatobenzene
  • Benzene, 1,2,4,5-tetrafluoro-3-isothiocyanato-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.