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151417-38-8

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151417-38-8 Usage

Description

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.

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.

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.

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.

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