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4-Phenylphenol

  • CAS:92-69-3
  • MF:C12H10O
  • Purity:99%
  • Molecular Weight:170.211
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Product Details

  • CAS: 92-69-3
  • MF: C12H10O
  • Appearance: Light tan solid (odour threshold detection limit 0.7 ppm)
  • Reputable manufacturer supply 4-Phenylphenol 92-69-3 in stock with high standard

    • Molecular Formula:C12H10O
    • Molecular Weight:170.211
    • Appearance/Colour:Light tan solid (odour threshold detection limit 0.7 ppm) 
    • Vapor Pressure:0.000428mmHg at 25°C 
    • Melting Point:164-166 °C(lit.) 
    • Refractive Index:1.604 
    • Boiling Point:306.387 °C at 760 mmHg 
    • PKA:9.55(at 25℃) 
    • Flash Point:147.175 °C 
    • PSA:20.23000 
    • Density:1.111 g/cm3 
    • LogP:3.05920 

    92-69-3 Relevant articles

    SYNTHESIS OF DIARYLS FROM PHENYLBORIC ACID AND ARYL IODIDES IN AN AQUEOUS MEDIUM

    Bumagin, N. A.,Bykov, V. V.,Beletskaya, I. P.

    , p. 2206 (1989)

    -

    Design of a capillary-microreactor for efficient Suzuki coupling reactions

    Basheer, Chanbasha,Jahir Hussain, Fathima Shahitha,Lee, Hian Kee,Valiyaveettil, Suresh

    , p. 7297 - 7300 (2004)

    A Pyrex glass capillary (0.4 mm internal...

    Selective heating of pd-modified ordered mesoporous carbon CMK-3 by microwave irradiation

    Inagaki, Satoshi,Onodera, Kenzo,Tani, Kensaku,Kubota, Yoshihiro

    , p. 1136 - 1143 (2011)

    Various microwave-heated heterogeneous c...

    Suzuki-miyaura reaction in water, catalyzed by palladium nanoparticles stabilized by pluronic F68 triblock copolymer

    Kashin,Beletskaya

    , p. 475 - 479 (2011)

    Palladium nanoparticles stabilized by Pl...

    One-pot hydrothermal synthesis of Pd/Fe3O4 nanocomposite in HEPES buffer solution and catalytic activity for Suzuki reaction

    Li, Shaozhong,Zhang, Wei,Chen, Fengxi,Chen, Rong

    , p. 186 - 191 (2015)

    The Pd/Fe3O4 nanocomposite integrates ve...

    Stabilized Palladium Nanoparticles: Synthesis, Multi-spectroscopic Characterization and Application for Suzuki–Miyaura Reaction

    Patel, Anish,Patel, Anjali

    , p. 3534 - 3547 (2018)

    The present article demonstrates a simpl...

    Highly active Pd-Ni nanocatalysts supported on multicharged polymer matrix

    Sultanova, Elza D.,Samigullina, Aida I.,Nastapova, Natalya V.,Nizameev, Irek R.,Kholin, Kirill V.,Morozov, Vladimir I.,Gubaidullin, Aidar T.,Yanilkin, Vitaliy V.,Kadirov, Marsil K.,Ziganshina, Albina Y.,Konovalov, Alexander I.

    , p. 5914 - 5919 (2017)

    In this article, we report the synthesis...

    Anchoring of palladium(II) in chemically modified mesoporous silica: An efficient heterogeneous catalyst for Suzuki cross-coupling reaction

    Bhunia, Susmita,Sen, Rupam,Koner, Subratanath

    , p. 3993 - 3999 (2010)

    The synthesis and characterization of a ...

    Magnetically recyclable Fe@Pd/C as a highly active catalyst for Suzuki coupling reaction in aqueous solution

    Tang, Weijie,Li, Jing,Jin, Xiaodong,Sun, Jian,Huang, Jingwei,Li, Rong

    , p. 75 - 78 (2014)

    In this work, a novel catalyst Fe@Pd/C w...

    Pd-sepiolite catalyst for Suzuki coupling reaction in water: Structural and catalytic investigations

    Shimizu, Ken-Ichi,Maruyama, Rei,Komai, Shin-Ichi,Kodama, Tatsuya,Kitayama, Yoshie

    , p. 202 - 209 (2004)

    [Pd(NH3)4]2+-exchanged sepiolite clay (P...

    Chitosan as a support for heterogeneous Pd catalysts in liquid phase catalysis

    Leonhardt, Silke E.S.,Stolle, Achim,Ondruschka, Bernd,Cravotto, Giancarlo,Leo, Cristina De,Jandt, Klaus D.,Keller, Thomas F.

    , p. 30 - 37 (2010)

    Four different chitosan-supported pallad...

    Imidazolium-urea low transition temperature mixtures for the UHP-promoted oxidation of boron compounds

    Martos, Mario,Pastor, Isidro M.

    , (2022/01/03)

    Different carboxy-functionalized imidazo...

    Research on the decomposition kinetics and thermal hazards of aniline diazonium salt

    Du, Lei,Wang, Ben,Xie, Chuanxin,Yuan, Yucan

    , (2022/01/22)

    Diazotization reaction, strong exothermi...

    An Imidazole-Rich Pd(II)-Polymer Pre-catalyst for the Suzuki-Miyaura Coupling: Stability Influenced by Dissolved Oxygen and Reactants Concentration

    Nishida, Elvis N.,Leopoldino, Elder C.,Zaramello, Laíze,Centurion, Higor A.,Gon?alves, Renato V.,Affeldt, Ricardo F.,Campos, Carlos E. M.,Souza, Bruno S.

    , (2022/02/01)

    Herein a novel Pd(II)-polymeric pre-cata...

    Production method and application of p-phenylphenol

    -

    Paragraph 0063; 0066-0070; 0071; 0074-0078; 0079; 0082-0086, (2022/03/27)

    The invention discloses a production met...

    92-69-3 Process route

    cyclohexanone
    108-94-1,11119-77-0,9003-41-2,9075-99-4

    cyclohexanone

    dibenzofuran
    132-64-9,214827-48-2

    dibenzofuran

    cyclohexenone
    930-68-7

    cyclohexenone

    2-Methylcyclopentanone
    1120-72-5

    2-Methylcyclopentanone

    diphenylether
    101-84-8

    diphenylether

    tert-butylbenzene
    253185-03-4,253185-04-5

    tert-butylbenzene

    biphenyl
    92-52-4,1594-86-1

    biphenyl

    propane
    74-98-6

    propane

    hexane
    110-54-3

    hexane

    n-hexan-2-one
    591-78-6

    n-hexan-2-one

    2-methyl-2-cyclopenten-1-one
    1120-73-6

    2-methyl-2-cyclopenten-1-one

    cyclohexane
    110-82-7,25012-93-5

    cyclohexane

    n-pentylcyclohexane
    4292-92-6

    n-pentylcyclohexane

    ethylbenzene
    100-41-4,27536-89-6

    ethylbenzene

    1-butylbenzene
    104-51-8

    1-butylbenzene

    pentylbenzene
    538-68-1

    pentylbenzene

    cyclopentylbenzene
    700-88-9

    cyclopentylbenzene

    4-Phenylphenol
    92-69-3

    4-Phenylphenol

    dicyclohexyl ether
    4645-15-2

    dicyclohexyl ether

    2-phenylpentane
    2719-52-0

    2-phenylpentane

    1-pentenylbenzene
    826-18-6

    1-pentenylbenzene

    2-butylcyclohexanone
    1126-18-7

    2-butylcyclohexanone

    cyclohexylphenyl ether
    2206-38-4

    cyclohexylphenyl ether

    2-cyclohexylphenol
    119-42-6

    2-cyclohexylphenol

    3-methyl-phenol
    108-39-4

    3-methyl-phenol

    ortho-cresol
    95-48-7,77504-84-8

    ortho-cresol

    2-Phenylphenol
    90-43-7,287950-96-3

    2-Phenylphenol

    toluene
    108-88-3,15644-74-3,16713-13-6

    toluene

    cyclohexene
    110-83-8

    cyclohexene

    cyclohexanol
    108-93-0

    cyclohexanol

    benzene
    71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1

    benzene

    phenol
    108-95-2,27073-41-2

    phenol

    Conditions
    Conditions Yield
    With hydrogen; 1 wtpercent K/1 wtpercent Pt/SiO2; at 425 ℃; under 5931.67 Torr;
    cyclohexanone
    108-94-1,11119-77-0,9003-41-2,9075-99-4

    cyclohexanone

    dibenzofuran
    132-64-9,214827-48-2

    dibenzofuran

    cyclohexenone
    930-68-7

    cyclohexenone

    2-Methylcyclopentanone
    1120-72-5

    2-Methylcyclopentanone

    diphenylether
    101-84-8

    diphenylether

    tert-butylbenzene
    253185-03-4,253185-04-5

    tert-butylbenzene

    biphenyl
    92-52-4,1594-86-1

    biphenyl

    propane
    74-98-6

    propane

    hexane
    110-54-3

    hexane

    cyclohexane
    110-82-7,25012-93-5

    cyclohexane

    ethylbenzene
    100-41-4,27536-89-6

    ethylbenzene

    pentylbenzene
    538-68-1

    pentylbenzene

    cyclopentylbenzene
    700-88-9

    cyclopentylbenzene

    4-Phenylphenol
    92-69-3

    4-Phenylphenol

    dicyclohexyl ether
    4645-15-2

    dicyclohexyl ether

    cyclohexylphenyl ether
    2206-38-4

    cyclohexylphenyl ether

    2-cyclohexylphenol
    119-42-6

    2-cyclohexylphenol

    ortho-cresol
    95-48-7,77504-84-8

    ortho-cresol

    2-Phenylphenol
    90-43-7,287950-96-3

    2-Phenylphenol

    toluene
    108-88-3,15644-74-3,16713-13-6

    toluene

    cyclohexene
    110-83-8

    cyclohexene

    cyclohexanol
    108-93-0

    cyclohexanol

    benzene
    71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1

    benzene

    phenol
    108-95-2,27073-41-2

    phenol

    Conditions
    Conditions Yield
    With hydrogen; 1 wtpercent K/1 wtpercent Pt/SiO2; at 425 ℃; under 5931.67 Torr;

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    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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