What is the 4-Benzoylbiphenyl?

4-Benzoylbiphenyl is off white crystalline powder, while it's Molecular Formula is C19H14O. off white crystalline powder 4-Benzoylbiphenyl is a reagent used in the synthesis of multicolored mechanochromic luminogen molecules.

What is the CAS number for 4-Benzoylbiphenyl?

The CAS number of 4-Benzoylbiphenyl is 2128-93-0.

What is 4-Benzoylbiphenyl (2128-93-0) used for?

4-Benzoylbiphenyl is a slightly yellow to beige crystalline powder that serves as a reagent in the synthesis of multicolored mechanochromic luminogen molecules.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

What is the 4-Benzoylbiphenyl?

4-Benzoylbiphenyl is off white crystalline powder, while it's Molecular Formula is C19H14O. off white crystalline powder 4-Benzoylbiphenyl is a reagent used in the synthesis of multicolored mechanochromic luminogen molecules.

What is the CAS number for 4-Benzoylbiphenyl?

The CAS number of 4-Benzoylbiphenyl is 2128-93-0.

What is 4-Benzoylbiphenyl (2128-93-0) used for?

4-Benzoylbiphenyl is a slightly yellow to beige crystalline powder that serves as a reagent in the synthesis of multicolored mechanochromic luminogen molecules.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

Excellent chemical plant bulk supply 4-Benzoylbiphenyl 2128-93-0

Product Details

Quick Details

CasNo： 2128-93-0
Molecular Formula： C₁₉H₁₄O
Appearance： off white crystalline powder
Purity： 99%

Excellent chemical plant bulk supply 4-Benzoylbiphenyl 2128-93-0

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

Uses	4-Benzoylbiphenyl was used in the synthesis of multicolored mechanochromic luminogen molecules. It also used in the adhesive manufacturing industry
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

Zhang, Peng,Weng, Zhihuan,Guo, Jia,Wang, Changchun

, 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

Lim, Kyoung-Chan,Hong, Young-Taek,Kim, Sunggak

, 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...

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, 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...

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

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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

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

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

2128-93-0 Process route

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

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

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

: 611-95-0
4-carboxybenzophenone

Conditions

Conditions	Yield

: 201230-82-2
carbon monoxide

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

: 98-80-6
phenylboronic acid

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

: 3016-97-5
1,4-dibenzoylbenzene

: 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

60-29-7
diethyl ether
32047-01-1
(2RS,3SR)-1-biphenyl-4-yl-2,3-epoxy-3-phenyl-propan-1-one
71-43-2
benzene
92-52-4
biphenyl

2128-93-0 Downstream products

65-85-0
benzoic acid
92-92-2
biphenyl-4-carboxylic acid
861622-18-6
Biphenyl-4-yl-phenyl-o-tolyl-methanol
40231-42-3
4-(1-phenylvinyl)-1,1′-biphenyl

;

2128-93-0

Quick Details

Excellent chemical plant bulk supply 4-Benzoylbiphenyl 2128-93-0

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

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)

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)

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

Zhang, Peng,Weng, Zhihuan,Guo, Jia,Wang, Changchun

, p. 5243 - 5249 (2011)

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

Lim, Kyoung-Chan,Hong, Young-Taek,Kim, Sunggak

, p. 1851 - 1854 (2006)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

2128-93-0 Process route

2128-93-0 Upstream products

2128-93-0 Downstream products

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