TR-D019130 - 4-11-difluoroethyl-1-fluoro-2-trifluoromethylbenzene | 1138445-20-1
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Trifluoromethylbenzene
CAS:Controlled ProductFormula:C7H5F3Color and Shape:NeatMolecular weight:146.111-Bromo-3-nitro-5-trifluoromethylbenzene
CAS:Formula:C7H3BrF3NO2Purity:98%Color and Shape:LiquidMolecular weight:270.00341-Benzyloxy-3-trifluoromethylbenzene
CAS:Formula:C14H11F3OColor and Shape:SolidMolecular weight:252.23171-Bromo-2-chloro-4-trifluoromethylbenzene
CAS:Formula:C7H3BrClF3Purity:98%Color and Shape:LiquidMolecular weight:259.45091,2-Difluoro-3-trifluoromethylbenzene
CAS:Formula:C7H3F5Purity:97%Color and Shape:LiquidMolecular weight:182.09071-Bromo-4-iodo-2-trifluoromethylbenzene
CAS:Formula:C7H3BrF3IPurity:97%Color and Shape:SolidMolecular weight:350.90241-Bromo-5-fluoro-4-nitro-2-trifluoromethylbenzene
CAS:1-Bromo-5-fluoro-4-nitro-2-trifluoromethylbenzenePurity:≥95%Molecular weight:287.99g/mol1-(2,2,2-Trifluoroethyl)-4-trifluoromethylbenzene
CAS:1-(2,2,2-Trifluoroethyl)-4-trifluoromethylbenzenePurity:95%Molecular weight:228.13g/mol4-Trifluoromethylbenzene-1-carbothioamide
CAS:<p>4-Trifluoromethylbenzene-1-carbothioamide (4FBA) is a non-toxic, organosulfur compound that is found in the fructus of Aurantii or Garcinia mangostana. 4FBA inhibits oxidant enzymes by reacting with their sulfhydryl groups and, as a result, prevents oxidation of other molecules. It has been shown to have antioxidant properties and inhibitory activity against two important enzymes that are involved in the progression of oxidative stress and inflammation. 4FBA has also been shown to be an effective inhibitor of chloride channels which may provide therapeutic potential for diseases such as sclerosis.</p>Formula:C8H6F3NSPurity:Min. 95%Color and Shape:PowderMolecular weight:205.2 g/mol3-Fluoro-5-nitro-1-trifluoromethylbenzene
CAS:Formula:C7H3F4NO2Purity:95%Color and Shape:LiquidMolecular weight:209.14-Trifluoromethylbenzene sulfonyl chloride
CAS:<p>4-Trifluoromethylbenzene sulfonyl chloride (TFB) is a functional group that is used as a ligand in some chemical reactions. TFB has been shown to be fluorescent, and can be used as a cancer cell marker. It also inhibits the growth of cancer cells by binding to their surface and inhibiting protein synthesis. 4-Trifluoromethylbenzene sulfonyl chloride can be synthesized by reacting ethylene with salicylic acid, followed by the reaction of the resulting ester with chloroform. This process yields TFB and chloride ions, which are then neutralized with sodium hydroxide to yield TFB sulfonate salt.</p>Formula:C7H4ClF3O2SPurity:Min. 95%Color and Shape:Colourless Or White To Light (Or Pale) Yellow To Brown SolidMolecular weight:244.62 g/mol3-Amino-4-(methylthio)benzotrifluoride
CAS:Formula:C8H8F3NSPurity:>98.0%(GC)(T)Color and Shape:Light yellow to Brown clear liquidMolecular weight:207.21Benzene, 1-chloro-2-fluoro-3-nitro-5-(trifluoromethyl)-
CAS:Formula:C7H2ClF4NO2Purity:98%Color and Shape:LiquidMolecular weight:243.54291,2-Difluoro-3-nitro-5-(trifluoromethyl)benzene
CAS:Formula:C7H2F5NO2Color and Shape:LiquidMolecular weight:227.0883Benzonitrile, 3-chloro-2-fluoro-5-(trifluoromethyl)-
CAS:Formula:C8H2ClF4NPurity:97%Color and Shape:LiquidMolecular weight:223.5548







