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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. Naphthol - Wikipedia

    en.wikipedia.org/wiki/Naphthol

    Download QR code; Print/export Download as PDF; Printable version; In other projects ... move to sidebar hide. Naphthol may refer to: 1-Naphthol; 2-Naphthol; This ...

  5. 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]

  6. Category:1-Naphthols - Wikipedia

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

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  7. Naphtholphthalein - Wikipedia

    en.wikipedia.org/wiki/Naphtholphthalein

    Download as PDF; Printable version; ... Interactive image; Beilstein Reference. ... Occupational safety and health (OHS/OSH): Main hazards.

  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 yellow S - Wikipedia

    en.wikipedia.org/wiki/Naphthol_yellow_S

    Naphthol yellow S is an organic compound that is a dye. It is a derivative of 1-naphthol . At one time it was a popular food colorant but it was delisted in 1959 in the U.S. [ 3 ]