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2,5-Diiodothieno[3,2-b]thiophene is an organic compound characterized by the molecular formula C6H2I2S2. It is a derivative of thieno[3,2-b]thiophene, featuring two iodine atoms attached to the thieno ring. 2,5-Diiodothieno[3,2-b]thiophene is known for its high electron mobility and strong absorption in the visible light region, which makes it a valuable material in the realm of organic electronics.

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  • 937187-29-6 Structure
  • Basic information

    1. Product Name: 2,5-Diiodothieno[3,2-b]thiophene
    2. Synonyms: 2,5-Diiodothieno[3,2-b]thiophene
    3. CAS NO:937187-29-6
    4. Molecular Formula: C6H2I2S2
    5. Molecular Weight: 392.01902
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 937187-29-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,5-Diiodothieno[3,2-b]thiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-Diiodothieno[3,2-b]thiophene(937187-29-6)
    11. EPA Substance Registry System: 2,5-Diiodothieno[3,2-b]thiophene(937187-29-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 937187-29-6(Hazardous Substances Data)

937187-29-6 Usage

Uses

Used in Organic Electronics Industry:
2,5-Diiodothieno[3,2-b]thiophene is utilized as a key component in the development of organic solar cells and field-effect transistors due to its high electron mobility and light absorption properties. Its ability to efficiently transport electrons and absorb light makes it a promising candidate for enhancing the performance of these devices.
Used in Organic Light-Emitting Diodes (OLEDs):
In the field of OLEDs, 2,5-Diiodothieno[3,2-b]thiophene is employed as a material to improve the efficiency and performance of light-emitting devices. Its strong light absorption and electron mobility contribute to the creation of OLEDs with better brightness, color quality, and energy efficiency.
Used in Organic Photodetectors:
2,5-Diiodothieno[3,2-b]thiophene has also been studied for its potential application in organic photodetectors. Its light absorption and electron transport properties make it suitable for the development of high-performance photodetectors that can detect and convert light into electrical signals effectively.

Check Digit Verification of cas no

The CAS Registry Mumber 937187-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,1,8 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 937187-29:
(8*9)+(7*3)+(6*7)+(5*1)+(4*8)+(3*7)+(2*2)+(1*9)=206
206 % 10 = 6
So 937187-29-6 is a valid CAS Registry Number.

937187-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-diiodothieno[3,2-b]thiophene

1.2 Other means of identification

Product number -
Other names -

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:937187-29-6 SDS

937187-29-6Upstream product

937187-29-6Relevant articles and documents

An efficient and regioselective iodination of electron-rich aromatic compounds using N-chlorosuccinimide and sodium iodide

Yamamoto, Takuya,Toyota, Kozo,Morita, Noboru

experimental part, p. 1364 - 1366 (2010/05/03)

An efficient and regioselective method for iodination of electron-rich aromatic compounds was found using N-chlorosuccinimide and sodium iodide in AcOH with short reaction times. This method is also applicable to non-benzenoid aromatic or heteroaromatic c

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