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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. Category:2-Naphthyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:2-Naphthyl_compounds

    This page was last edited on 8 November 2022, at 18:36 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  4. 1-Naphthalenethiol - Wikipedia

    en.wikipedia.org/wiki/1-Naphthalenethiol

    1-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 2-naphthalenethiol .

  5. 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 ...

  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. 2-Naphthoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Naphthoic_acid

    2-Naphthoic acid is an organic compound of the formula C 10 H 7 CO 2 H. It is one of two isomeric carboxylic acid derivatives of naphthalene , the other one being 1-naphthoic acid . It can be prepared by carboxylation of 1-chloronaphthalene .

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 It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds.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

    en.wikipedia.org/wiki/Diisopropylnaphthalenes

    Diisopropylnaphthalenes (DIPN) is a solvent for carbonless copy paper.The oil consists of a mixture of isomers of diisopropylnaphthalene.Some key properties are broad liquid range, low volatility, and low toxicity.