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  2. Biphenyl - Wikipedia

    en.wikipedia.org/wiki/Biphenyl

    Biphenyl (also known as diphenyl, phenylbenzene, 1,1′-biphenyl, lemonene [4] or BP) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl .

  3. Biphenyl synthase - Wikipedia

    en.wikipedia.org/wiki/Biphenyl_synthase

    In enzymology, a biphenyl synthase (EC 2.3.1.177) is an enzyme that catalyzes the chemical reaction: . 3 malonyl-CoA + benzoyl-CoA 4 CoA + 3,5-dihydroxybiphenyl + 4 CO 2. Thus, the two substrates of this enzyme are malonyl-CoA and benzoyl-CoA, whereas its three products are CoA, 3,5-dihydroxybiphenyl, and CO 2.

  4. 4-Cyano-4'-pentylbiphenyl - Wikipedia

    en.wikipedia.org/wiki/4-Cyano-4'-pentylbiphenyl

    4-Cyano-4'-pentylbiphenyl is a commonly used nematic liquid crystal with the chemical formula C 18 H 19 N. It frequently goes by the common name 5CB. 5CB was first synthesized by George William Gray, Ken Harrison, and J.A. Nash at the University of Hull in 1972 and at the time it was the first member of the cyanobiphenyls.

  5. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    The bisphenols (/ ˈ b ɪ s f ɪ n ɒ l /) are a group of industrial chemical compounds related to diphenylmethane; commonly used in the creation of plastics and epoxy resins. [ 1 ] [ 2 ] [ 3 ] Most are based on two hydroxyphenyl functional groups linked by a methylene bridge .

  6. 4,4'-Biphenol - Wikipedia

    en.wikipedia.org/wiki/4,4'-Biphenol

    The industrial synthesis of 4,4′-biphenol was developed by Allan Hay in the 1960s. [ 2 ] [ 3 ] As the direct oxidative coupling of phenol gives a mixture of isomers, [ 4 ] [ 5 ] 4,4′-biphenol is instead prepared from 2,6-di-tert-butylphenol , where para-coupling is the only possibility. [ 3 ]

  7. Dihydroxybiphenyl - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybiphenyl

    3 Synthesis and applications. 4 Safety ... refers to a class of organic compounds consisting of a biphenyl structure with two hydroxyl groups attached. The most ...

  8. Diphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Diphenylmethane

    The acidity of the methylene group in diphenylmethane is due to the weakness of the (C 6 H 5) 2 CH–H bond, which has a bond dissociation energy of 82 kcal mol −1 (340 kJ mol −1). [5] This is well below the published bond dissociation energies for comparable C–H bonds in propane , where BDE((CH 3 ) 2 CH–H)=98.6 kcal mol −1 , and ...

  9. Chemical synthesis - Wikipedia

    en.wikipedia.org/wiki/Chemical_synthesis

    Organic synthesis is a special type of chemical synthesis dealing with the synthesis of organic compounds. For the total synthesis of a complex product, multiple procedures in sequence may be required to synthesize the product of interest, needing a lot of time. A purely synthetic chemical synthesis begins with basic lab compounds.