CAS 17417-09-3: 2-fluoro-5-nitrobenzonitrile
Formula:C8H4F3NS
InChI:InChI=1/C8H4F3NS/c9-8(10,11)6-3-1-2-4-7(6)12-5-13/h1-4H
SMILES:c1ccc(c(c1)C(F)(F)F)N=C=S
Synonyms:- 1-Isothiocyanato-2-(Trifluoromethyl)Benzene
Sort by
Found 8 products.
2-Fluoro-5-nitrobenzonitrile
CAS:Purity:99.0%Color and Shape:SolidMolecular weight:166.110992431640622-Fluoro-5-nitrobenzonitrile, 98+%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H3FN2O2Purity:98+%Color and Shape:White to cream to yellow, PowderMolecular weight:166.11Benzonitrile, 2-fluoro-5-nitro-
CAS:Formula:C7H3FN2O2Purity:98%Color and Shape:SolidMolecular weight:166.10932-Fluoro-5-nitrobenzonitrile
CAS:2-Fluoro-5-nitrobenzonitrile is a reactive chemical that has been used to study the interaction of amines with nitro groups. It can react with serine protease and acetylcholine, forming a lactam intermediate. The reaction of 2-fluoro-5-nitrobenzonitrile with hydrogen peroxide produces oxygen gas, water, and nitrous acid. The reaction of 2-fluoro-5-nitrobenzonitrile with benzamidine produces phenylhydrazine and benzoic acid. This chemical has shown anti-cancer activity in cell culture studies, as well as inhibition of cancer cell growth in vivo. 2-Fluoro-5-nitrobenzonitrile is also an inhibitor of the enzyme nitric oxide synthase (NOS). It reacts with the heme group in NOS, which prevents the formation of NO from L-arginine.Formula:C7H3FN2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:166.11 g/mol2-Fluoro-5-nitrobenzonitrile
CAS:Formula:C7H3FN2O2Purity:>97.0%(GC)Color and Shape:White to Yellow to Green powder to crystalMolecular weight:166.112-Fluoro-5-nitrobenzonitrile
CAS:2-Fluoro-5-nitrobenzonitrileFormula:C7H3FN2O2Purity:95%Color and Shape: white solidMolecular weight:166.11g/mol
