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  2. 2-Naphthol - Wikipedia

    en.wikipedia.org/wiki/2-Naphthol

    The OH→Br conversion has been described. [5] Electrophilic attack occurs characteristically at the 1-position as indicated by nitrosylation to give 1-nitroso-2-naphthol. [6] Bromination [7] and alkylations proceed with similar regiochemistry. [8] Ring-opening reactions have been documented. [9] Carbonation of 2-naphthol gives 2-hydroxy-1 ...

  3. 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 .

  4. Acid Orange 7 - Wikipedia

    en.wikipedia.org/wiki/Acid_Orange_7

    Toggle the table of contents. ... Interactive image; ChemSpider: 21171709 ... Acid Orange 7, also known as 2-naphthol orange is an azo dye. It is used for dyeing wool.

  5. 2-Methoxynaphthalene - Wikipedia

    en.wikipedia.org/wiki/Β-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. Category:2-Naphthols - Wikipedia

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

    This page was last edited on 14 November 2024, at 15:03 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. Naphthol - Wikipedia

    en.wikipedia.org/wiki/Naphthol

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide. Naphthol may refer to: 1-Naphthol; 2-Naphthol; This page was ...

  8. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichloro-5,6-dicyano-1...

    The reagent removes pairs of H atoms from organic molecules. The stoichiometry of its action is illustrated by the conversion of tetralin to naphthalene: 2 C 6 Cl 2 (CN) 2 O 2 + C 10 H 12 → 2 C 6 Cl 2 (CN) 2 (OH) 2 + C 10 H 8. The resulting hydroquinone is poorly soluble in typical reaction solvents (dioxane, benzene, alkanes), which ...

  9. 1,1′-Bi-2-naphthol - Wikipedia

    en.wikipedia.org/wiki/1,1′-Bi-2-naphthol

    1,1 ′-Bi-2-naphthol (BINOL) is an organic compound that is often used as a ligand for transition-metal catalysed asymmetric synthesis. BINOL has axial chirality and the two enantiomers can be readily separated and are stable toward racemisation .