• soluble
  • The present invention relates to a solvent-soluble aniline conducting polymer, a method for producing the same, a conductive composition with the same, an electric conductor formed from the conductive composition and a method for producing the same. (google.com)
  • acid
  • Chromic acid converts it into quinone, whereas chlorates, in the presence of certain metallic salts (especially of vanadium), give aniline black. (wikipedia.org)
  • Potassium permanganate in neutral solution oxidizes it to nitrobenzene, in alkaline solution to azobenzene, ammonia and oxalic acid, in acid solution to aniline black. (wikipedia.org)
  • For example, reaction of aniline with sulfuric acid at 180 °C produces sulfanilic acid, H2NC6H4SO3H. (wikipedia.org)
  • N-Methylation of aniline with methanol at elevated temperatures over acid catalysts gives N-methylaniline and dimethylaniline: C6H5NH2 + 2 CH3OH → C6H5N(CH3)2 + 2H2O N-Methylaniline and dimethylaniline are colorless liquids with boiling points of 193-195 °C and 192 °C, respectively. (wikipedia.org)
  • The first compound of the homolog row of nitriles, the nitrile of formic acid, hydrogen cyanide was first synthesized by C. W. Scheele in 1782. (wikipedia.org)
  • Trees and woody plants are killed by a complex group of factors that include parasites, such as fungus and beetles, pollution, such as acid rain and organic compounds, and drought. (wikipedia.org)
  • methyl
  • Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. (wikipedia.org)
  • reaction
  • The imine in this organic reaction is a condensation reaction product from an aniline type compound and a benzaldehyde type compound. (wikipedia.org)
  • The largest scale industrial reaction of aniline involves its alkylation with formaldehyde. (wikipedia.org)
  • Commercially available, this compound may be used as a building block, e.g. in the preparation of p-bromobiphenyl via the Gomberg-Bachmann reaction. (wikipedia.org)
  • conversion to an ortho-aminothiol through the Herz-reaction (aniline 5 and disulfur dichloride), followed by conversion to an ortho-aminoarylthioglycolacid and conversion of the aromatic amine function to a nitrile via the Sandmeyer reaction. (wikipedia.org)
  • This compound is converted to 7 via a ring-closing reaction and decarboxylation. (wikipedia.org)
  • Horseradish peroxidase has an accessible active site, and many compounds can reach the site of the reaction. (wikipedia.org)
  • benzene
  • Traditionally, the weak basicity of aniline is attributed to a combination of inductive effect from the more electronegative sp2 carbon and resonance effects, as the lone pair on the nitrogen is partially delocalized into the pi system of the benzene ring. (wikipedia.org)
  • The NH2 group attached to the benzene ring means that there is a lone pair of electrons that can enter into conjugation with the benzene ring resulting in delocalization in the aniline. (wikipedia.org)
  • Oxidation
  • The oxidation of aniline has been heavily investigated, and can result in reactions localized at nitrogen or more commonly results in the formation of new C-N bonds. (wikipedia.org)
  • variety
  • Certain intermediates, e.g. the 3-(iodoalkyl) compounds, were converted to a variety of (3-substituted-alkyl)-EMAUs by displacement. (umassmed.edu)
  • industrial
  • This approach not only provides more insight into the origin of life but also offers a pathway to acquire enantiopure compounds for industrial applications. (nih.gov)
  • Several
  • Several compounds protected mice from lethal intraperitoneal (ip) infections with S. aureus (Smith) when given by the ip route. (umassmed.edu)
  • bond
  • The existence of metal-nitrogen bond for all pyridine and aniline complexes, except H 2 CdI 4 ·4 An ( An =aniline), is adduced from infrared and far infrared spectral studies. (springer.com)