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2,2'-[(Z)-1,2-Ethenediyl]bisthiophene, a chemical compound with the molecular formula C10H6S2, is a bisthiophene derivative characterized by two thiophene rings connected by an ethylene group in a cis configuration. 2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is known for its unique electronic properties, making it a valuable component in the field of organic synthesis and materials science.

22769-07-9

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22769-07-9 Usage

Uses

Used in Organic Synthesis:
2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is used as a key intermediate in organic synthesis for the preparation of various functional organic molecules, leveraging its distinctive electronic characteristics to enhance the properties of the synthesized compounds.
Used in Organic Electronic Devices:
In the Organic Electronics Industry, 2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is utilized as a crucial component in the fabrication of organic light-emitting diodes (OLEDs) due to its ability to improve device performance and efficiency.
Used in Organic Photovoltaic Cells:
2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is employed as a material in organic photovoltaic cells (OPVs) for its potential to enhance light absorption and charge transport, contributing to the overall efficiency of solar energy conversion.
Used in Organic Field-Effect Transistors:
In the realm of Organic Field-Effect Transistors (OFETs), 2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is used as a semiconductor material, capitalizing on its electronic properties to achieve improved transistor performance.
Used in Solar Cells:
2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is investigated for its potential use in solar cells, where it may contribute to the development of more efficient and cost-effective photovoltaic technologies by improving light absorption and charge separation.
Used in Sensors:
2,2'-[(Z)-1,2-Ethenediyl]bisthiophene is also being explored for its application in sensors, where its electronic properties could be harnessed to create sensitive and selective detection mechanisms for various analytes.
Overall, 2,2'-[(Z)-1,2-Ethenediyl]bisthiophene's versatility in multiple applications across different industries is a testament to its significance in advancing the capabilities of organic materials in modern technology.

Check Digit Verification of cas no

The CAS Registry Mumber 22769-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22769-07:
(7*2)+(6*2)+(5*7)+(4*6)+(3*9)+(2*0)+(1*7)=119
119 % 10 = 9
So 22769-07-9 is a valid CAS Registry Number.

22769-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3,3-dithienylethene

1.2 Other means of identification

Product number -
Other names 1,3-Di-(2-thienyl)-aethylen

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:22769-07-9 SDS

22769-07-9Downstream Products

22769-07-9Relevant academic research and scientific papers

Unexpected rearrangement during the gas-phase dehalogenation approach to benzodithiophenes

Aitken, R. Alan,Oyewale, Adebayo O.

, p. 19379 - 19381 (2015/04/14)

A range of halogenated methylthiophenes undergo dehalogenative condensation upon FVP over magnesium or calcium to give products including benzodithiophenes; in some cases this involves a novel rearrangement by equilibration of alkenylthienyl radicals via thiophene-fused cyclopropylmethyl intermediates. This journal is

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