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2128-93-0

  • Product Name4-Benzoylbiphenyl
  • MFC19H14O
  • Molecular Weight258.32
  • Purity99%
  • Appearanceoff white crystalline powder
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Product Details

Quick Details

  • CasNo： 2128-93-0
  • MF： C19H14O
  • Appearance： off white crystalline powder
  • Purity： 99%

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  • Molecular Formula:C19H14O
  • Molecular Weight:258.32
  • Appearance/Colour:off white crystalline powder 
  • Vapor Pressure:3.11E-07mmHg at 25°C 
  • Melting Point:99-101 °C 
  • Refractive Index:1.609 
  • Boiling Point:419.1 °C at 760 mmHg 
  • Flash Point:190.7 °C 
  • PSA：17.07000 
  • Density:1.266 g/cm3 
  • LogP:4.58460 

4-Benzoylbiphenyl(Cas 2128-93-0) Usage

Chemical Properties

SLIGHTLY YELLOW TO BEIGE CRYSTALLINE POWDER

Uses

4-Benzoylbiphenyl is a reagent used in the synthesis of multicolored mechanochromic luminogen molecules.

Flammability and Explosibility

Notclassified

InChI:InChI=1/C19H14O/c20-19(17-9-5-2-6-10-17)18-13-11-16(12-14-18)15-7-3-1-4-8-15/h1-14H

2128-93-0 Relevant articles

Self-Supported Ligands as a Platform for Catalysis: Use of a Polymeric Oxime in a Recyclable Palladacycle Precatalyst for Suzuki-Miyaura Reactions

Yang, Yun-Chin,Toy, Patrick H.

, p. 1319 - 1324 (2014)

A self-supported oxime palladacycle prec...

Synthesis and characterization of Pd-γ-Fe2O3 nanocomposite and its application as a magnetically recyclable catalyst in ligand-free Suzuki-Miyaura reaction in water

Paul, Dipankar,Rudra, Siddheswar,Rahman, Prabin,Khatua, Snehadrinarayan,Pradhan, Mukul,Chatterjee, Paresh Nath

, p. 96 - 102 (2018)

A novel redox-driven method to synthesiz...

Solution-dispersible, colloidal, conjugated porous polymer networks with entrapped palladium nanocrystals for heterogeneous catalysis of the Suzuki-Miyaura coupling reaction

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, p. 5243 - 5249 (2011)

Conjugated nanoporous polymer colloids (...

Carboxylic phosphoric anhydrides as a new coupling partner in Pd-catalyzed coupling reactions: A new ketone synthesis

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, p. 1851 - 1854 (2006)

The Pd-catalyzed cross-coupling reaction...

Modified zeolite immobilized palladium for ligand-free Suzuki-Miyaura cross-coupling reaction

Kumbhar, Arjun,Kamble, Santosh,Mane, Anand,Jha, Ratnesh,Salunkhe, Rajashri

, p. 29 - 34 (2013)

A palladium-based catalyst supported on ...

Ultra-small palladium nano-particles synthesized using bulky S/Se and N donor ligands as a stabilizer: Application as catalysts for Suzuki-Miyaura coupling

Oswal, Preeti,Arora, Aayushi,Kaushal, Jolly,Rao, Gyandshwar Kumar,Kumar, Sushil,Singh, Ajai K.,Kumar, Arun

, p. 22313 - 22319 (2019)

Two chalcogenated ligands L1 and L2 cont...

Controlled Synthesis of Palladium Nanocubes as an Efficient Nanocatalyst for Suzuki-Miyaura Cross-Coupling and Reduction of p-Nitrophenol

Bhavya, M.,Bhol, Prangya,Kandathil, Vishal,Patil, Siddappa A.,Samal, Akshaya K.,Swain, Swarnalata

, p. 5208 - 5218 (2020)

Anisotropic nanocatalysts have attracted...

Direct synthesis of ferrocenylmethylphosphines from ferrocenylmethyl alcohols and their application as ligands for room temperature Pd(0)-catalyzed Suzuki cross-couplings of aryl bromides

Tang, Zhen-Yu,Lu, Yong,Hu, Qiao-Sheng

, p. 297 - 300 (2003)

(Matrix presented) The direct, high-yiel...

Catalytic reactivity of the complexes [Pd{(Ph2P)2N(tBu)-P,P′}X2], X = Cl, Br, I, in the Suzuki-Miyaura C?C coupling reaction: Probing effects of the halogeno ligand X? and the ligand's tBu group

Ioannou, Polydoros-Chrysovalantis,Arbez-Gindre, Cécile,Zoumpanioti, Maria,Raptopoulou, Catherine P.,Psycharis, Vassilis,Kostas, Ioannis D.,Kyritsis, Panayotis

, p. 40 - 46 (2019)

The synthesis, as well as the spectrosco...

Reusable magnetic Pd:XCoy nanoalloys confined in mesoporous carbons for green Suzuki-Miyaura reactions

Enneiymy, Mohamed,Le Drian, Claude,Matei Ghimbeu, Camélia,Becht, Jean-Michel

, p. 17176 - 17182 (2018)

We report herein PdxCoy nanoalloys confi...

Suzuki?Miyaura coupling and O?arylation reactions catalysed by palladium(II) complexes of bulky ligands bearing naphthalene core, Schiff base functionality and biarylphosphine moiety

Arora, Aayushi,Kaushal, Jolly,Kumar, Arun,Nautiyal, Divyanshu,Oswal, Preeti,Singh, Siddhant

, (2022/01/19)

Schiff bases L1 [i.e., 2-(diphenylphosph...

Identification and optimization of biphenyl derivatives as novel tubulin inhibitors targeting colchicine-binding site overcoming multidrug resistance

Cheng, Bao,Zhu, Guirong,Meng, Linghua,Wu, Guolin,Chen, Qin,Ma, Shengming

, (2021/11/22)

Microtubule targeting agents (MTAs) are ...

Mechanochemical Solvent-Free Suzuki–Miyaura Cross-Coupling of Amides via Highly Chemoselective N?C Cleavage

Ma, Yangmin,Shao, Lei,Szostak, Michal,Wang, Ruihong,Zhang, Jin,Zhang, Pei

supporting information, (2022/01/04)

Although cross-coupling reactions of ami...

Selective Activation of Unstrained C(O)-C Bond in Ketone Suzuki-Miyaura Coupling Reaction Enabled by Hydride-Transfer Strategy

Zhong, Jing,Zhou, Wuxin,Yan, Xufei,Xia, Ying,Xiang, Haifeng,Zhou, Xiangge

, p. 1372 - 1377 (2022/02/23)

A Rh(I)-catalyzed ketone Suzuki-Miyaura ...

2128-93-0 Process route

1-(4-biphenyl)-1,2,2-triphenylethylene
70592-08-4

1-(4-biphenyl)-1,2,2-triphenylethylene

acetic acid
64-19-7,77671-22-8

acetic acid

biphenyl-4-yl-phenyl-methanone
2128-93-0

biphenyl-4-yl-phenyl-methanone

4-carboxybenzophenone
611-95-0

4-carboxybenzophenone

Conditions
Conditions Yield
carbon monoxide
201230-82-2

carbon monoxide

para-diiodobenzene
624-38-4,1032416-46-8

para-diiodobenzene

phenylboronic acid
98-80-6

phenylboronic acid

biphenyl-4-yl-phenyl-methanone
2128-93-0

biphenyl-4-yl-phenyl-methanone

1,4-dibenzoylbenzene
3016-97-5

1,4-dibenzoylbenzene

[1,1';4',1'']terphenyl
92-94-4,94363-13-0

[1,1';4',1'']terphenyl

Conditions
Conditions Yield
With palladium diacetate; sodium carbonate; In water; at 100 ℃; for 6h; under 760.051 Torr; Sealed tube; Autoclave; Green chemistry;
63 %Spectr.
22 %Spectr.
15 %Spectr.

2128-93-0 Upstream products

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    diethyl ether

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    benzene

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    92-52-4

    biphenyl

2128-93-0 Downstream products

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    benzoic acid

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