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  2. Naphthalene poisoning - Wikipedia

    en.wikipedia.org/wiki/Naphthalene_poisoning

    Naphthalene is a major component of some mothballs.It repels moths as well as some animals. [citation needed]Since mothballs that contain naphthalene are considered hazards, safer alternatives have been developed, such as the use of 1,4-dichlorobenzene, however, 1,4-dichlorobenzene has been declared as a potential neurotoxin. 1,4-dichlorobenzene has been linked to potentially causing ...

  3. 1-Naphthol - Wikipedia

    en.wikipedia.org/wiki/1-naphthol

    1-Naphthol, or α-naphthol, is an organic compound with the formula C 10 H 7 OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are ...

  4. Naphthalene - Wikipedia

    en.wikipedia.org/wiki/Naphthalene

    Naphthalenesulfonic acids are used in the synthesis of 1-naphthol and 2-naphthol, precursors for various dyestuffs, pigments, rubber processing chemicals and other chemicals and pharmaceuticals. [25] They are also used as dispersants in synthetic and natural rubbers, in agricultural pesticides , in dyes, and in lead–acid battery plates.

  5. Category:1-Naphthols - Wikipedia

    en.wikipedia.org/wiki/Category:1-Naphthols

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  6. Carbaryl - Wikipedia

    en.wikipedia.org/wiki/Carbaryl

    Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]

  7. N-(1-Naphthyl)ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N-(1-Naphthyl)ethylenediamine

    N-(1-Naphthyl)ethylenediamine dihydrochloride is widely used in the quantitative analysis of nitrate and nitrite in water samples by colorimetry. It readily undergoes a diazonium coupling reaction in the presence of nitrite to give a strongly colored azo compound .

  8. 1,4-Naphthoquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-Naphthoquinone

    1,4-Naphthoquinone acts as strong dienophile in Diels-Alder reaction.Its adduct with 1,3-butadiene can be prepared by two methods: 1) long (45 days) exposure of naphthoquinone in neat liquid butadiene taken in huge excess at room temperature in a thick-wall glass tube or 2) fast catalyzed cycloaddition at low temperature in the presence of 1 equivalent of tin(IV) chloride: [5]

  9. Naphthol - Wikipedia

    en.wikipedia.org/wiki/Naphthol

    English. Read; Edit; View history; Tools. Tools. move to sidebar hide. Actions Read; ... Naphthol may refer to: 1-Naphthol; 2-Naphthol This page was last edited on 26 ...