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92-69-3

  • Product Name4-Phenylphenol
  • Molecular FormulaC12H10O
  • Molecular Weight170.211
  • Purity99%
  • AppearanceLight tan solid (odour threshold detection limit 0.7 ppm)
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Product Details

Quick Details

  • CasNo: 92-69-3
  • Molecular Formula: C12H10O
  • Appearance: Light tan solid (odour threshold detection limit 0.7 ppm)
  • Purity: 99%

Top quality factory supply 92-69-3 4-Phenylphenol at low price

  • 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...

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...

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...

Synthesis of Fluorenes and Dibenzo[ g,p]chrysenes through an Oxidative Cascade

Dickinson, Cody F.,Tius, Marcus A.,Yap, Glenn P. A.

supporting information, p. 1559 - 1563 (2022/02/07)

We have developed robust, operationally ...

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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