612-71-5

  • Product Name:1,3,5-Triphenylbenzene
  • Molecular Formula:C24H18
  • Purity:99%
  • Molecular Weight:306.407
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Product Details;

CasNo: 612-71-5

Molecular Formula: C24H18

Appearance: LIGHT BROWN /CRYSTALLINE POWDER

factory and supplier 612-71-5 1,3,5-Triphenylbenzene in stock

  • Molecular Formula:C24H18
  • Molecular Weight:306.407
  • Appearance/Colour:LIGHT BROWN /CRYSTALLINE POWDER 
  • Vapor Pressure:3.31E-08mmHg at 25°C 
  • Melting Point:172-174 °C(lit.) 
  • Refractive Index:1.4800 (estimate) 
  • Boiling Point:460 °C(lit.) 
  • Flash Point:238 ºC 
  • PSA:0.00000 
  • Density:1.074 g/cm3 
  • LogP:6.68760 

1,3,5-Triphenylbenzene(Cas 612-71-5) Usage

Purification Methods

Purify it by chromatography on alumina using *benzene or pet ether as eluents. Crystallise the triphenylbenzene from EtOH (m 174o). [Beilstein 5 H 737, 5 I 370, 5 II 670, 5 III 2563, 5 IV 2732.]

InChI:InChI=1/C24H18/c1-4-10-19(11-5-1)22-16-23(20-12-6-2-7-13-20)18-24(17-22)21-14-8-3-9-15-21/h1-18H

612-71-5 Relevant articles

Efficient conversion of acetophenones into 1,3,5-triarylbenzenes catalyzed by bismuth(III) trifluoromethanesulfonate tetrahydrate

Ono, Fumiaki,Ishikura, Yuichi,Tada, Yuusuke,Endo, Masato,Sato, Tsuneo

, p. 2365 - 2367 (2008)

Bismuth(III) trifluoromethanesulfonate t...

Highly efficient and novel method for synthesis of 1,3,5-triarylbenzenes from acetophenones

Phatangare, Kiran,Padalkar, Vikas,Mhatre, Devidas,Patil, Ketan,Chaskar, Atul

, p. 4117 - 4121 (2009)

Heteropolyacid-phosphomolybdic acid has ...

Thionyl chloride-catalyzed preparation of microporous organic polymers through aldol condensation

Zhao, Yan-Chao,Zhou, Ding,Chen, Qi,Zhang, Xin-Jian,Bian, Ning,Qi, Ai-Di,Han, Bao-Hang

, p. 6382 - 6388 (2011)

We demonstrated the synthesis of five ki...

1,3,5-triphenylbenzene as unexpected by-product in the synthesis of 2,5-diphenylpyrrole from acetophenone oxime and phenylacetylene

Shmidt,Zorina,Mikhaleva,Ushakov,Skital'Tseva,Trofimov

, p. 457 - 458 (2010)

-

Efficient one-step synthesis of C 3-symmetrical benzenoid compounds mediated by SOCl 2/EtOH

Zhao, Sanhu,Kang, Lina,Ge, Haixia,Yang, Feifei,Wang, Chenlu,Li, Chang,Wang, Qiang,Zhao, Minggen

, p. 3569 - 3578 (2012)

An efficient one-step synthesis of branc...

Independent electrocyclization and oxidative chain cleavage along the backbone of cis-poly(phenylacetylene)

Percec, Virgil,Rudick, Jonathan G.

, p. 7241 - 7250 (2005)

cis-Poly(phenylacetylene) (PPA) and cis-...

TiCl3(OTf) catalyses the efficient conversion of acetophenones to 1,3,5-triaryl benzenes

Iranpoor,Zeynizaded

, p. 1079 - 1080 (1998)

The quantitative conversion of different...

Simple and convenient synthesis of 1,3,5-triarylbenzenes from ketones

Hu, Anan,Zhang, Anjiang,Ding, Lisheng,Lei, Xinxiang,Zhang, Lixue

, p. 720 - 721 (2007)

A new and efficient synthesis of a serie...

Silver(I) Interactions with Ketones. Site of Complexation with Acetophenones and Effectiveness as a Lewis Acid Catalyst

Crist, DeLanson R.,Hsieh, Zon-Hong,Quicksall, Carl O.,Sun, Michael K.

, p. 2478 - 2483 (1984)

Aromatic ketones present three possible ...

OLIGOMERISATION OF PHENYL ACETYLENE OVER TITANIUM OXIDE SUPPORTED ON SILICA - ALUMINA CATALYST

Kumar, V. G.,Shoba, T. S.,Rao, K. V. C.

, p. 6245 - 6248 (1985)

Titanium oxide on silica-alumina support...

2-cyano-iso-propyl radical addition to alkynes

Montevecchi, Pier Carlo,Navacchia, Maria Luisa,Spagnolo, Piero

, p. 7929 - 7936 (1997)

The thermolysis of azobisisobutyronitril...

Fabrication of palladium nanoparticles as effective catalysts by using supramolecular gels

Zhang, Wei,Xie, Zhi-Gang

, p. 77 - 80 (2016)

Two-component supramolecular gels were m...

Chiral diphosphine derivatives of alkylidyne tricobalt carbonyl clusters - A comparative study of different cobalt carbonyl (pre)catalysts for (asymmetric) intermolecular Pauson-Khand reactions

Mottalib, M. Abdul,Haukka, Matti,Nordlander, Ebbe

, p. 275 - 282 (2016)

Reaction of the tricobalt carbyne cluste...

SRN1 and stille reactions: A new synthetic strategy

Corsico, Eduardo F.,Rossi, Roberto A.

, p. 431 - 432 (2000)

The photostimulated reaction of Me3Sn- i...

Catalytic three-component coupling of alkynes, imines, and organoboron reagents

Patel, Sejal J.,Jamison, Timothy F.

, p. 1364 - 1367 (2003)

An unusual degree of functional group co...

A facile synthesis of 1,3,5-triaryl benzenes from acetophenone diethyl ketals in the presence of acetyl chloride and SmCl3

Cheng, Ke-Jun,Ding, Zong-Biao,Wu, Shi-Hui

, p. 11 - 15 (1997)

Samarium trichloride, SmCl3, has been fo...

Effect of phosphonium ionic liquid/Pd ratio on the catalytic activity of palladium nanoparticles in Suzuki cross-coupling reaction

Arkhipova, D.,Ermolaev, V.,Gaynanova, G.,Hey-Hawkins, E.,Miluykov, V.,Oeckler, O.,Wagner, G.,Zakharova, L.

, (2020)

Phosphonium salts were synthesized and u...

Suzuki cross-coupling of hexachlorobenzene promoted by the Buchwald ligands

Burukin, A. S.,Vasil’ev, A. A.,Zhdankina, G. M.,Zlotin, S. G.

, p. 169 - 172 (2022/02/17)

The study of cross-coupling between hexa...

Variation on the π-Acceptor Ligand within a RhI?N-Heterocyclic Carbene Framework: Divergent Catalytic Outcomes for Phenylacetylene-Methanol Transformations

Galiana-Cameo, María,Passarelli, Vincenzo,Pérez-Torrente, Jesús J.,Di Giuseppe, Andrea,Castarlenas, Ricardo

, p. 2947 - 2957 (2021/07/16)

A series of neutral and cationic rhodium...

Hydrogen-Bonding Controlled Nickel-Catalyzed Regioselective Cyclotrimerization of Terminal Alkynes

Yang, Kai,Wang, Pengfei,Sun, Ze-Ying,Guo, Minjie,Zhao, Wentao,Tang, Xiangyang,Wang, Guangwei

supporting information, p. 3933 - 3938 (2021/05/26)

Herein we report a hydrogen-bonding cont...

Iron-catalyzed trimerization of terminal alkynes enabled by pyrimidinediimine ligands: A regioselective method for the synthesis of 1,3,5-substituted arenes

Doll, Julianna S.,Eichelmann, Robert,Hertwig, Leif E.,Bender, Thilo,Kohler, Vincenz J.,Bill, Eckhard,Wadepohl, Hubert,Ro?ca, Drago?-Adrian

, p. 5593 - 5600 (2021/05/31)

The development of pyrimidine-based anal...

612-71-5 Process route

2,4,6-Triphenyl,4'-methylbenzophenone
130894-36-9

2,4,6-Triphenyl,4'-methylbenzophenone

terephthalic acid
100-21-0

terephthalic acid

1,3,5-triphenylbenzene
612-71-5

1,3,5-triphenylbenzene

p-Toluic acid
99-94-5

p-Toluic acid

Conditions
Conditions Yield
at 275 - 285 ℃;
bis(η6-diphenyl)chromium(0)
12099-15-9

bis(η6-diphenyl)chromium(0)

bis(toluene)chromium<sup>(0)</sup>
12087-58-0

bis(toluene)chromium(0)

C<sub>6</sub>H<sub>6</sub>CrC<sub>6</sub>H<sub>5</sub>C<sub>2</sub>H<sub>5</sub>
32875-80-2

C6H6CrC6H5C2H5

2-Ethyltoluene
611-14-3

2-Ethyltoluene

ortho-diethylbenzene
253185-02-3,135-01-3

ortho-diethylbenzene

1,3,5-triphenylbenzene
612-71-5

1,3,5-triphenylbenzene

Conditions
Conditions Yield
Friedel-Crafts synthesis; chromy.;
Friedel-Crafts synthesis; chromy.;

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