enow.com Web Search

  1. Ads

    related to: 4 phenyl benzene sulfonyl chloride solution for dogs

Search results

  1. Results from the WOW.Com Content Network
  2. Benzenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonyl_chloride

    The compound is prepared by the chlorsulfonation of benzene: C 6 H 6 + 2SHO 3 SCl → C 6 H 5 SO 2 Cl + HCl + SO 3. Benzenesulfonic acid is an intermediate in this conversion. Diphenylsulfone is a side product. Benzenesulfonyl chloride can also be prepared by treating benzenesulfonate salts with phosphorus oxychloride. [2]

  3. Benzenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonic_acid

    Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.It is the simplest aromatic sulfonic acid.It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether.

  4. Phenylsulfinic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylsulfinic_acid

    C 6 H 5 SO 2 Cl + Na 2 SO 3 + H 2 O → C 6 H 5 SO 2 H + NaCl + NaHSO 4. Many other methods have been reported for production of sulfinic acids such as the use tin(II) chloride, or the Grignard reagent with sulfur dioxide. [4] The preparation of sulfinic acids by the oxidation of thiols is difficult due to overoxidation.

  5. Hinsberg reaction - Wikipedia

    en.wikipedia.org/wiki/Hinsberg_reaction

    The Hinsberg reaction is a chemical test for the detection of primary, secondary and tertiary amines.The reaction was first described by Oscar Hinsberg in 1890. [1] [2] In this test, the amine is shaken well with the Hinsberg reagent (benzenesulfonyl chloride) in the presence of aqueous alkali (either KOH or NaOH).

  6. Diphenylamine - Wikipedia

    en.wikipedia.org/wiki/Diphenylamine

    Diphenylamine is an organic compound with the formula (C 6 H 5) 2 NH. The compound is a derivative of aniline, consisting of an amine bound to two phenyl groups. The compound is a colorless solid, but commercial samples are often yellow due to oxidized impurities. [5]

  7. Polysulfone - Wikipedia

    en.wikipedia.org/wiki/Polysulfone

    The original synthesis of PAES involved electrophilic aromatic substitution of an diaryl ether with the bis (sulfonyl chloride) of benzene. Reactions typically use a Friedel-Crafts catalyst, such as ferric chloride or antimony pentachloride: n O(C 6 H 5) 2 + n SO2Cl2 → {[O(C 6 H 4) 2]SO 2} n + 2n HCl

  1. Ads

    related to: 4 phenyl benzene sulfonyl chloride solution for dogs