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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 ...
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]
Naphthol may refer to: 1-Naphthol; 2-Naphthol This page was last edited on 26 June 2023, at 00:21 (UTC). Text is available under the Creative Commons Attribution ...
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]
With NaOH, converts to 5-amino-1-naphthol ("purpurol"). 1-Aminonaphthalene-6-sulfonic acid: 119-79-9: 1,6-Cleve’s acid (named after swedish chemist Per Teodor Cleve) sulfonation of 1-aminonaphthalene: 1-Aminonaphthalene-7-sulfonic acid: 119-28-8: 1,7-Cleve’s acid: by-product in production of 1,6-Cleve’s acid, precursor to C.I. Acid Black ...
2-Naphthol, or β-naphthol, is a fluorescent colorless (or occasionally yellow) crystalline solid with the formula C 10 H 7 OH. It is an isomer of 1-naphthol , differing by the location of the hydroxyl group on the naphthalene ring.
N-(1-Naphthyl)ethylenediamine is an organic compound. It is commercially available as part of Griess reagents, which find application in quantitative inorganic analysis of nitrates , nitrite and sulfonamide in blood, using the Griess test .
1-Nitroso-2-naphthol can be prepared by treatment of 2-naphthol with nitrous acid: [3] C 10 H 7 OH + HNO 2 → C 10 H 6 (NO)OH + H 2 O. Its conjugate base forms deeply colored complexes with iron(II) and cobalt(II), complexes [M(C 10 H 6 (NO)O) 3] 2-. [4] The deep colors of these complexes results from the delocalized bonding within each five ...