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  2. Biphenyl - Wikipedia

    en.wikipedia.org/wiki/Biphenyl

    C 6 H 5 CH 3 + C 6 H 6 → C 6 H 5 −C 6 H 5 + CH 4. The other principal route is by the oxidative dehydrogenation of benzene: 2 C 6 H 6 + ½ O 2 → C 6 H 5 −C 6 H 5 + H 2 O. Annually 40,000,000 kg are produced by these routes. [9] In the laboratory, biphenyl can also be synthesized by treating phenylmagnesium bromide with copper(II) salts.

  3. 1-Boc-4-AP - Wikipedia

    en.wikipedia.org/wiki/1-Boc-4-AP

    1-Boc-4-AP (tert-butyl 4-(phenylamino)piperidine-1-carboxylate) is a compound used as an intermediate in the manufacture of fentanyl, as well as various related derivatives such as butyrylfentanyl, furanylfentanyl, benzylfentanyl and homofentanyl, among others.

  4. Metal–organic framework - Wikipedia

    en.wikipedia.org/wiki/Metal–organic_framework

    The 3D framework [Cu 3 (btc) 2 (H 2 O) 3] (btc: benzene-1,3,5-tricarboxylate) used in this study was first reported by Williams et al. [67] The open framework of [Cu 3 (btc) 2 (H 2 O) 3] is built from dimeric cupric tetracarboxylate units (paddle-wheels) with aqua molecules coordinating to the axial positions and btc bridging ligands. The ...

  5. Diallyl carbonate - Wikipedia

    en.wikipedia.org/wiki/Diallyl_carbonate

    The monomer (1,1'-biphenyl)-4,4'-diallylcarbonate is synthesized by reacting 4,4'-biphenyl, pyridine, and allyl chlorocarbonate at 5°C. Simultaneously, the monomer hexa(4-allylcarbonatephenoxy)cyclotriphosphazene is prepared by the reaction of Allyl(4-hydroxyphenyl) carbonate with hexachlorocyclotriphosphazene.

  6. Biphenol - Wikipedia

    en.wikipedia.org/wiki/Biphenol

    2,2'-Biphenol (RN 1806-29-7) m.p. 109 °C; 3,3'-Biphenol (RN 612-76-0) m.p. 124.8 °C; 4,4'-Biphenol (RN 92-88-6) m.p. 283 °C; Additionally, three unsymmetrical isomers of biphenol exist: 2,3'-Biphenol (RN 31835-45-7) 2,4'-Biphenol (RN 611-62-1) m.p. 162-163 °C; 3,4'-Biphenol (RN 18855-13-5) m.p. 190 °C

  7. 4-Nitrobiphenyl - Wikipedia

    en.wikipedia.org/wiki/4-Nitrobiphenyl

    4-Nitrobiphenyl is an organic compound with the formula C 6 H 5 −C 6 H 4 NO 2. It is one of three isomers of nitrobiphenyl and probably the most widely used. It is a precursor to the antioxidant 4-aminobiphenyl. 4-Nitrobiphenyl is readily prepared by nitration of biphenyl. [1] It can also be prepared by cross-coupling reactions. [2]

  8. 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]

  9. Dihydroxybiphenyl - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybiphenyl

    Dihydroxybiphenyl (as known as biphenol) refers to a class of organic compounds consisting of a biphenyl structure with two hydroxyl groups attached. The most common isomers are 2,2'-dihydroxybiphenyl and 4,4'-dihydroxybiphenyl.

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