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19053-14-6

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19053-14-6 Usage

General Description

4,4''-Diiodo-p-terphenyl is a chemical compound consisting of two phenyl rings linked by a central benzene ring, with each of the phenyl rings having iodine substituents at the 4 positions. It is a symmetrical molecule with high molecular weight and is commonly used as a dopant in the fabrication of organic semiconductors for electronic devices. The presence of the iodine atoms provides the compound with unique optical and electronic properties, making it suitable for various applications in the field of organic electronics. Additionally, 4,4''-Diiodo-p-terphenyl has also been studied for its potential use in photonic and optoelectronic devices due to its strong absorption and emission properties in the ultraviolet-visible range. It is important to handle this compound with appropriate safety measures due to its toxic and potentially hazardous nature.

Check Digit Verification of cas no

The CAS Registry Mumber 19053-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19053-14:
(7*1)+(6*9)+(5*0)+(4*5)+(3*3)+(2*1)+(1*4)=96
96 % 10 = 6
So 19053-14-6 is a valid CAS Registry Number.

19053-14-6 Well-known Company Product Price

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  • TCI America

  • (D3534)  4,4''-Diiodo-p-terphenyl  >98.0%(GC)

  • 19053-14-6

  • 1g

  • 990.00CNY

  • Detail
  • TCI America

  • (D3534)  4,4''-Diiodo-p-terphenyl  >98.0%(GC)

  • 19053-14-6

  • 5g

  • 2,990.00CNY

  • Detail

19053-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(4-iodophenyl)benzene

1.2 Other means of identification

Product number -
Other names 4,4''-diiodoterphenyl

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:19053-14-6 SDS

19053-14-6Relevant articles and documents

Synthesis of dicyanomethyl and nitro substituted p-polyphenyls and their salts

Zauhar,Bandrauk,Truong,Michel

, p. 703 - 706 (1995)

A one-step, medium-scale synthesis of several novel dicyanomethyl and nitro substituted p-polyphenyls from 4,4'- or 4''-diiodo-parapolyphenyls and from 4-iodo-4'- or 4''-nitro-p-polyphenyls, respectively, and sodium malononitrile using a palladium catalys

AROMATIC AMINE DERIVATIVE, AND ORGANIC ELECTROLUMINESCENCE ELEMENT USING THE SAME

-

Paragraph 0314-0315, (2016/10/17)

Of a specific structure novel aromatic amine derivatives, and at least a light-emitting layer between a cathode and an anode including 1 layer or an organic thin film composed of one layer interposed in an organic electroluminescent element, said organic thin film least 1 layer, hole transport layer in particular said aromatic amine derivatives by itself or as a component of a mixture by, whether or not result in crystallization of molecules, organic electroluminescent device corresponding to a predetermined liquid crystal and, tube having a long lifetime in organic electroluminescent device with high.

Synthesis and functional properties of symmetrically naphthyl-Based oligoarylenes with high glass-transition temperatures

Zhang, Xiaolinga,Sun, Kanga,Liu, Yurong,Xiong, Mojunb,Xia, Pingfanga,Li, Zhonghui,Cao, Zijian

experimental part, p. 1034 - 1040 (2010/10/18)

Symmetrically naphthyl-based π-conjugated oligoarylenes, OPP(4)Ph-TNp, OPP(4)An-TNp and OPP(4)OXTNp have successfully been synthesized by a divergent approach using Pd-catalyzed Suzuki cross-coupling reaction of diiodo- or dibromo-oligoarylene and arylboronic acid as a key step. Their optical, electrochemical and thermal properties have also been characterized. These newly synthesized naphthyl-based oligoarylenes show highly morphological (Tg 149-187 °C) and thermal (Tdec 509-597 °C) stabilities as well as exhibit potential applications in optoelectronic fields.

AROMATIC AMINE DERIVATIVE, AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME

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Page/Page column 23, (2009/04/23)

A novel aromatic amine derivative which is a diamine compound having a p-terphenyl-4,4"-diyl structure. An organic electroluminescence device which is composed of one or more organic thin film layers including at least one light emitting layer sandwiched

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