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  2. Iron gall ink - Wikipedia

    en.wikipedia.org/wiki/Iron_gall_ink

    1 g carbolic acid (phenol, C 6 H 5 OH, biocide) (preservative) 3.5 g china-blue aniline dye (water-soluble) 1000 cm 3 distilled water [21] The Popular Science iron gall writing ink article also mentions methyl violet dye could be used to make a violet iron gall ink without revealing the amount and soluble nigrosine dye for an immediate black ...

  3. 2-Aminothiophenol - Wikipedia

    en.wikipedia.org/wiki/2-Aminothiophenol

    2-Aminothiophenol can prepared in two steps, starting with the reaction of aniline with carbon disulfide followed by hydrolysis of the resulting mercaptobenzothiazole. [1] It can also obtained by zinc reduction of 2-nitrobenzene sulfonyl chloride .

  4. Aniline - Wikipedia

    en.wikipedia.org/wiki/Aniline

    Aniline (from Portuguese anil 'indigo shrub', and -ine indicating a derived substance) [6] is an organic compound with the formula C 6 H 5 NH 2. Consisting of a phenyl group ( −C 6 H 5 ) attached to an amino group ( −NH 2 ), aniline is the simplest aromatic amine .

  5. Aminophenol - Wikipedia

    en.wikipedia.org/wiki/Aminophenol

    They are simultaneously an aniline and a phenol This page was last edited on 19 November 2024, at ...

  6. Phenol oxidation with hypervalent iodine reagents - Wikipedia

    en.wikipedia.org/wiki/Phenol_oxidation_with...

    Substrates containing two phenols (or an aniline and a phenol; see equation (8) below for a related example), undergo oxidative coupling in the presence of hypervalent iodine(III) reagents. Coupling of both the ortho and para positions is possible; however, the use of bulky silyl-protected phenols provides complete selectivity for para coupling ...

  7. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    A nucleophilic aromatic substitution (S N Ar) is a substitution reaction in organic chemistry in which the nucleophile displaces a good leaving group, such as a halide, on an aromatic ring.

  8. Betti reaction - Wikipedia

    en.wikipedia.org/wiki/Betti_reaction

    Once the imine is produced, it reacts with phenol in the presence of water to yield an α-aminobenzylphenol. An electron pushing mechanism for the Betti Reaction. First, the lone-pair on the nitrogen of the imine deprotonates the phenol, pushing the bonding electrons onto the oxygen.

  9. 3-Aminophenol - Wikipedia

    en.wikipedia.org/wiki/3-Aminophenol

    One of the most relevant applications of the substance is the synthesis of 3-(diethylamino)phenol, key intermediate for the preparation of several fluorescent dyes (e.g., rhodamine B). Other uses for the compound include hair dye colorants and stabilizers for chlorine-containing thermoplastics. [4]