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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. Openclipart - Wikipedia

    en.wikipedia.org/wiki/Openclipart

    Openclipart, also called Open Clip Art Library, is an online media repository of free-content vector clip art.The project hosts over 160,000 free graphics and has billed itself as "the largest community of artists making the best free original clipart for you to use for absolutely any reason".

  4. 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 ...

  5. File:Walmart logo.svg - Wikipedia

    en.wikipedia.org/wiki/File:Walmart_logo.svg

    2009-09-06 20:57 Griffin5 190×50× (7876 bytes) Reverted to version as of 00:15, 27 July 2009; 2009-09-06 20:57 Griffin5 268×67× (9800 bytes) Reverted to version as of 18:46, 15 August 2008

  6. 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 .

  7. File:Naphthalene 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:Naphthalene_200.svg

    The following other wikis use this file: Usage on ar.wikipedia.org مركب حلقي; Usage on be.wikipedia.org Нафталін; Usage on bg.wikipedia.org

  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 It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds.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-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 ...