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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 prepared from 2-naphthol by the Newman–Kwart rearrangement starting from a thiocarbamate. [1] It undergoes lithiation at the 1 and 3-position. [2] [3] It can be used as a flavouring agent and has been described as having an “artichoke”, “meaty” and “creamy” taste”. [4] [5]

  4. 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 ...

  5. Acid Orange 7 - Wikipedia

    en.wikipedia.org/wiki/Acid_Orange_7

    Toggle the table of contents. ... Download as PDF; Printable version; In other projects ... 2-naphthol orange, Orange II, CI 15510, D&C Orange 4, COLIPA C015 ...

  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. C10H8O - Wikipedia

    en.wikipedia.org/wiki/C10H8O

    Download as PDF; Printable version ... C 10 H 8 O may refer to: Naphthols. 1-Naphthol; 2-Naphthol; Benzoxepins. 1-Benzoxepin ... This page was last edited on 5 ...

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