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  2. 2-Naphthalenethiol - Wikipedia

    en.wikipedia.org/wiki/2-Naphthalenethiol

    2-Naphthalenethiol is an organosulfur compound with the formula C 10 H 7 SH. It is a white solid. It is a white solid. It is one of two mono thiols of naphthalene , the other being 1-naphthalenethiol .

  3. 2-Naphthol - Wikipedia

    en.wikipedia.org/wiki/2-Naphthol

    Traditionally, 2-naphthol is produced by a two-step process that begins with the sulfonation of naphthalene in sulfuric acid: [2] C 10 H 8 + H 2 SO 4 → C 10 H 7 SO 3 H + H 2 O. The sulfonic acid group is then cleaved in molten sodium hydroxide: C 10 H 7 (SO 3 H) + 3 NaOH → C 10 H 7 ONa + Na 2 SO 3 + 2 H 2 O. Neutralization of the product ...

  4. Naphthenic oil - Wikipedia

    en.wikipedia.org/wiki/Naphthenic_oil

    The UOP characterisation factor (K w) (UOP 375-07 [2]), is based on the observation that the specific gravities of the hydrocarbons are related to their H/C ratio (and thus to their chemical character) and that their boiling points are linked to their number of carbon atoms in their molecules. High values of Kw (13-12.5) indicate a ...

  5. 2-Methoxynaphthalene - Wikipedia

    en.wikipedia.org/wiki/2-Methoxynaphthalene

    2-Methoxynaphthalene, also called β-naphthol methyl ether or yara yara, [2] is a stabilizer found in gunpowder, particularly smokeless gunpowders. It is soluble in alcohol , and insoluble in water and dipropylene glycol .

  6. 1-Naphthalenethiol - Wikipedia

    en.wikipedia.org/wiki/1-Naphthalenethiol

    [1] 1-Naphthalenethiol can also be prepared from 1-bromonaphthalene by Pd-catalyzed reaction with the silylthiolate i Pr 3 SiSK followed by hydrolysis of the silathioether. [2] It was first prepared from the Grignard reagent generated from 1-bromonaphthalene. Treatment of that reagent with elemental sulfur followed by acidification gave the ...

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  8. 2-Naphthylamine - Wikipedia

    en.wikipedia.org/wiki/2-Naphthylamine

    2-Naphthylamine or 2-aminonaphthalene is one of two isomeric aminonaphthalenes, compounds with the formula C 10 H 7 NH 2. It is a colorless solid, but samples take on a reddish color in air because of oxidation. It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds. [2]

  9. 2,6-Dimethylnaphthalene - Wikipedia

    en.wikipedia.org/wiki/2,6-Dimethylnaphthalene

    2,6-Dimethylnaphthalene is mainly used for the preparation of 2,6-naphthalenedicarboxylic acid by oxidation of 2,6-dimethylnaphthalene in the liquid phase. 2,6-Naphthalenedicarboxylic acid is a monomer for the production of high-performance polymers, in particular poly (ethylene-2,6-naphthalene dicarboxylate) or shorter polyethylene naphthalate (PEN). [4]