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  2. Triphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanol

    Triphenylmethanol (also known as triphenylcarbinol and TrOH) is an organic compound. It is a white crystalline solid that is insoluble in water and petroleum ether , but well soluble in ethanol , diethyl ether , and benzene .

  3. 2-Naphthol - Wikipedia

    en.wikipedia.org/wiki/2-Naphthol

    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.

  4. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  5. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    (C 6 H 5) 3 CCl + 2 Na → (C 6 H 5) 3 CNa + NaCl. The use of tritylsodium as a strong, non-nucleophilic base has been eclipsed by the popularization of butyllithium and related strong bases. The unmodified anion is red, and can be used as an indicator in acid–base titrations. Derived substances have proven useful as chemical dyes.

  6. 2-Methoxynaphthalene - Wikipedia

    en.wikipedia.org/wiki/2-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 .

  7. 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 .

  8. Aminonaphthalenesulfonic acids - Wikipedia

    en.wikipedia.org/wiki/Aminonaphthalenesulfonic_acids

    2-Aminonaphthalene-1-sulfonic acid: 81-16-3: Tobias acid: Bucherer reaction of 2-hydroxynaphthalene-1-sulfonic acid with ammonium salts, precursor to C.I. Pigment Red 49 2-Aminonaphthalene-5-sulfonic acid: 81-05-0: Dahl’s acid, Dressel acid, D acid: Desulfonation of 2-aminonaphthalene-1,5-disulfonic acid 2-Aminonaphthalene-6-sulfonic acid: 93 ...

  9. Triphenylmethyl chloride - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_chloride

    Melting point: 109 to 112 °C (228 to 234 °F; 382 to 385 K) ... It may be prepared by the reaction of triphenylmethanol with acetyl chloride, ... 2 (C 6 H 5) 3 CCl ...