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1,3,5-Tris(4-iodophenyl)benzene, also known as 90, is an organic compound with a unique structure consisting of a benzene ring with three 4-iodophenyl groups attached to it. 1 3 5-TRIS(4-IODOPHENYL)BENZENE) 90 is characterized by its symmetrical arrangement and the presence of iodine atoms, which may contribute to its potential applications in various fields.

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  • 151417-38-8 Structure
  • Basic information

    1. Product Name: 1 3 5-TRIS(4-IODOPHENYL)BENZENE) 90
    2. Synonyms: 1 3 5-TRIS(4-IODOPHENYL)BENZENE) 90;4,4''-Diiodo-5'-(4-iodophenyl)-1,1':3',1''-terphenyl;1,3,5-Tris(4-iodophenyl)benzene 97%;tert-butyl 3-iodoindazole-1-carboxylate
    3. CAS NO:151417-38-8
    4. Molecular Formula: C24H15I3
    5. Molecular Weight: 684.08
    6. EINECS: 1308068-626-2
    7. Product Categories: Organic Electronics and Photonics;Synthetic Intermediates;Synthetic Tools and Reagents
    8. Mol File: 151417-38-8.mol
  • Chemical Properties

    1. Melting Point: 254-260 °C(lit.)
    2. Boiling Point: 600.262 °C at 760 mmHg
    3. Flash Point: 309.929 °C
    4. Appearance: /
    5. Density: 1.946 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 1 3 5-TRIS(4-IODOPHENYL)BENZENE) 90(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1 3 5-TRIS(4-IODOPHENYL)BENZENE) 90(151417-38-8)
    11. EPA Substance Registry System: 1 3 5-TRIS(4-IODOPHENYL)BENZENE) 90(151417-38-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 41
    3. Safety Statements: 26-39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 151417-38-8(Hazardous Substances Data)

151417-38-8 Usage

Uses

Used in Chemical Synthesis:
1,3,5-Tris(4-iodophenyl)benzene 90 is used as a building block in the synthesis of C3-symmetric nano-sized polyaromatics and molecular propellers. Its unique structure and the presence of iodine atoms make it a valuable component in the creation of complex organic molecules with specific properties and potential applications in various industries.
Used in Pharmaceutical Industry:
1,3,5-Tris(4-iodophenyl)benzene 90 can be utilized as a starting material or intermediate in the development of new pharmaceutical compounds. Its structural features may be exploited to design and synthesize novel drugs with improved efficacy and selectivity.
Used in Material Science:
The compound may also find applications in the field of material science, particularly in the development of new materials with specific optical, electronic, or mechanical properties. The presence of iodine atoms and the symmetrical arrangement of the phenyl groups could contribute to the unique characteristics of the resulting materials.

Check Digit Verification of cas no

The CAS Registry Mumber 151417-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,1 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151417-38:
(8*1)+(7*5)+(6*1)+(5*4)+(4*1)+(3*7)+(2*3)+(1*8)=108
108 % 10 = 8
So 151417-38-8 is a valid CAS Registry Number.

151417-38-8 Well-known Company Product Price

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  • Aldrich

  • (656453)  1,3,5-Tris(4-iodophenyl)benzene  90%

  • 151417-38-8

  • 656453-1G

  • 2,156.31CNY

  • Detail
  • Aldrich

  • (656453)  1,3,5-Tris(4-iodophenyl)benzene  90%

  • 151417-38-8

  • 656453-5G

  • 7,581.60CNY

  • Detail

151417-38-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Tris(4-iodophenyl)benzene

1.2 Other means of identification

Product number -
Other names 4,4''-Diiodo-5'-(4-iodophenyl)-1,1':3',1''-terphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:151417-38-8 SDS

151417-38-8Relevant articles and documents

Synthesis of C3-Symmetric star-shaped molecules containing 1,3-azoles via hetero-aryl Heck coupling

Kotha, Sambasivarao,Todeti, Saidulu

, p. 1359 - 1363 (2019/02/06)

We have demonstrated a useful synthetic strategy to assemble star-shaped C3-symmetric molecules containing 1,3-azole moieties at the periphery. To generate these C3-symmetric heterocycles, we have employed the Pd/Cu-based coupling reactions. To this end, we have used benzoxazole, benzothiazole, and benzimidazole as coupling partners to generate the corresponding hetero-aryl Heck coupling products.

Synthesis of C3-symmetric star-shaped molecules containing α-amino acids and dipeptides via Negishi coupling as a key step

Kotha, Sambasivarao,Todeti, Saidulu

, p. 371 - 377 (2019/02/20)

We demonstrate a new synthetic strategy toward star-shaped C3-symmetric molecules containing α-amino acid (AAA) derivatives and dipeptides. In this regard, trimerization and Negishi cross-coupling reactions are used as the key steps starting fr

Selective and reversible interconversion of nanosliders commanded by remote control: Via metal-ion signaling

Saha, Suchismita,Biswas, Pronay Kumar,Paul, Indrajit,Schmittel, Michael

supporting information, p. 14733 - 14736 (2019/12/24)

A multi-device network mainly consisting of two two-component nanosliders was formed by self-sorting of six components. Addition/removal of zinc(ii) ions reversibly reorganized the network by chemical signaling involving the translocation of copper(i) from a relay station followed by the selective disassembly/assembly of one of both multi-component devices. The thus liberated machine parts served to erect a three-component nanoslider alongside the other unchanged two-component nanoslider.

Electrical and electrochemical properties of lithium solvated electron solutions derived from 1,3,5-triphenylbenzenes

Lunchev, Andrey V.,Tan, Kim Seng,Grimsdale, Andrew C.,Yazami, Rachid

supporting information, p. 15678 - 15683 (2018/10/04)

A series of 1,3,5-triphenylbenzenes (TPBs) bearing various substituents have been made and their ability to form lithium solvated electron solutions (LiSESs) in tetrahydrofuran (THF) solution have been studied. It was found that the TPBs bearing electron

Sulfated tungstate catalyzed synthesis of C3-symmetric 1,3,5-triaryl benzenes under solvent-free condition

Wagh, Ganesh D.,Akamanchi, Krishnacharya G.

supporting information, p. 3032 - 3036 (2017/07/17)

Sulfated tungstate catalyzed environmentally benign, simple, one pot, and solvent-free method has been developed for the synthesis of 1,3,5-triarylbenzenes via cyclic self-condensation of three molecules of aryl ketones. High yields, short reaction time, easy work-up procedure and recycling of the catalyst endorse advantage.

Structure-property relationships of star-shaped blue-emitting charge-transporting 1,3,5-triphenylbenzene derivatives

Kukhta, Nadzeya A.,Volyniuk, Dmytro,Peciulyte, Laura,Ostrauskaite, Jolita,Juska, Gytis,Grazulevicius, Juozas V.

, p. 122 - 132 (2015/03/18)

Three star-shaped derivatives of 1,3,5-triphenylbenzene bonded to fluorene moieties with various linking groups were designed and synthesized. The three dendritic compounds are characterized by high values of decomposition temperature (up to 434 °C) and f

Alcohol-soluble electron-transport small molecule for fully solution-processed multilayer white electrophosphorescent devices

Jiang, Wei,Xu, Huange,Ban, Xinxin,Yuan, Guolong,Sun, Yueming,Huang, Bin,Duan, Lian,Qiu, Yong

supporting information, p. 1140 - 1143 (2014/03/21)

A novel alcohol-soluble electron-transport material was designed and synthesized. This material not only possesses a high triplet energy and a low HOMO level but also exhibits excellent electron-transport properties and good film-forming ability. Efficien

Novel self-assembled 2D networks based on zinc metal ion co-ordination: Synthesis and comparative study with 3D networks

Rajwar, Deepa,Liu, Xinfeng,Lim, Zheng Bang,Cho, Sung Ju,Chen, Shi,Thomas, Jens M. H.,Trewin, Abbie,Lam, Yeng Ming,Sum, Tze Chien,Grimsdale, Andrew C.

, p. 17680 - 17693 (2014/05/06)

The synthesis of linear and trigonal terpyridine bearing molecules (tpys) and their self-assembly to form novel extended self-assembled 2D networks of trigonal tpys with linear tpys through zinc metal ion (Zn2+) co-ordination is reported. The r

Modular syntheses of star-shaped pyridine, bipyridine, and terpyridine derivatives by employing sonogashira reactions

Trawny, Daniel,Kunz, Valentin,Reissig, Hans-Ulrich

supporting information, p. 6295 - 6302 (2015/03/30)

A simple and flexible synthesis for a series of star-shaped pyridine, bipyridine, and terpyridine derivatives is reported by using a modular approach that combines the use of a ligand, spacer, and core unit. A fairly efficient method to prepare 4′-nonafloxy-functionalized terpyridine derivatives is described. The building blocks that contain the functionalized pyridine, bipyridine, or terpyridine derivatives were linked to different C3-symmetrical core units. In most cases, Sonogashira reactions were employed in the crucial final steps of the synthesis. A star-shaped dodecafluorinated compound was also prepared in a straightforward fashion. A simple procedure for the preparation of partially silylated 1,3,5-triethynylbenzene derivatives is presented, which provides an approach to C2-symmetrical star-shaped compounds that have only one terpyridine and two terphenyl units as "dummy" ligands. The absorption and emission spectra of the fully conjugated C3-symmetrical pyridine derivatives were systematically investigated, and fairly large Stokes shifts were observed.

Highly efficient synthesis of substituted benzenes in the presence of B(HSO4)3 as a new and reusable catalyst under solvent-free conditions

Safaei, Hamid Reza,Davoodi, Mansooreh,Shekouhy, Mohsen

supporting information, p. 2178 - 2190 (2013/07/19)

A highly efficient and simple procedure for the synthesis of substituted benzenes is described. A broad range of ketones (alkyl-aryl ketones and cyclic ketones) were condensed via a cyclotrimerization reaction in the presence of catalytic amounts of boron sulfonic acid [B(HSO4)3], a new, highly efficient, and reusable catalyst, under solvent-free conditions. All reactions completed in short times without formation of any by-products. The catalyst was recovered and reused successfully for 15 cycles of the reaction. Copyright

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