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  2. 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 .

  3. 1-Naphthalenethiol - Wikipedia

    en.wikipedia.org/wiki/1-Naphthalenethiol

    [1] 1-Naphthalenethiol can also be prepared from 1-bromonaphthalene by Pd-catalyzed reaction with the silylthiolate i Pr 3 SiSK followed by hydrolysis of the silathioether. [2] It was first prepared from the Grignard reagent generated from 1-bromonaphthalene. Treatment of that reagent with elemental sulfur followed by acidification gave the ...

  4. 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 .

  5. 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.

  6. 2-Naphthoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Naphthoic_acid

    2-Naphthoic acid is an organic compound of the formula C 10 H 7 CO 2 H. It is one of two isomeric carboxylic acid derivatives of naphthalene , the other one being 1-naphthoic acid . It can be prepared by carboxylation of 1-chloronaphthalene .

  7. Aminonaphthalenesulfonic acids - Wikipedia

    en.wikipedia.org/wiki/Aminonaphthalenesulfonic_acids

    Aminonaphthalenesulfonic acids are compounds with the composition C 10 H 6 (NH 2)(SO 3 H), being derived from naphthalene (C 10 H 8) substituted by an amino and sulfonic acid groups. These compounds are colorless solids.

  8. 2,6-Naphthalenedicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/2,6-Naphthalenedi...

    It was first prepared by Robert Evert and Victor Merz in 1876 by hydrolysis of 2,6-dicyanonaphthalene. [2] [3] 1,8-Naphthalenedicarboxylic acid can be isomerized to 2,6-naphthalenedicarboxylic acid via the intermediacy of the dipotassium dicarboxylates. [2] It is also produced by oxidation of 2,6-diisopropylnaphthalene. [4]

  9. Naphthalene 1,2-dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Naphthalene_1,2-dioxygenase

    The 4 substrates of this enzyme are naphthalene, NADH, H +, and O 2, whereas its two products are (1R,2S)-1,2-dihydronaphthalene-1,2-diol and NAD +. This enzyme belongs to the family of oxidoreductases , specifically those acting on paired donors, with O2 as oxidant and incorporation or reduction of oxygen.