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2,6-Diphenylbenzo[1,2-b:4,5-b']difuran is a complex organic compound characterized by a unique structure that features two phenyl rings attached to a benzene core, which is fused to two furan rings. This molecule is known for its potential applications in various chemical and pharmaceutical industries due to its specific electronic and steric properties. The compound's structure provides it with a range of chemical reactivity and stability, which can be exploited in the synthesis of more complex molecules or as a component in materials science. Its chemical formula is C24H14O2, reflecting the presence of carbon, hydrogen, and oxygen atoms in its structure. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the phenyl and furan moieties, making it a subject of interest for researchers exploring its potential uses in various fields.

5379-77-1

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5379-77-1 Usage

Uses

Used in Organic Electronics:
2,6-Diphenylbenzo[1,2-b:4,5-b']difuran is used as a semiconductor material for its potential applications in organic electronics. Its unique structure and electronic properties make it a candidate for further research and development in this field.
Used in Optoelectronics:
In the optoelectronics industry, 2,6-Diphenylbenzo[1,2-b:4,5-b']difuran is used as a component in devices that rely on the interaction of light with electronic components. Its optical properties are of interest for enhancing the performance of such devices.
Used in Organic Light-Emitting Diodes (OLEDs):
2,6-Diphenylbenzo[1,2-b:4,5-b']difuran is used as a component in OLEDs for its potential to improve the efficiency and performance of these display technologies.
Used in Organic Photovoltaic Cells (OPVs):
2,6-Diphenylbenzo[1,2-b:4,5-b']difuran is utilized as a material in OPVs, where its semiconducting properties can contribute to the generation of electricity from light.
Used in Organic Field-Effect Transistors (OFETs):
2,6-Diphenylbenzo[1,2-b:4,5-b']difuran is used in the development of OFETs, where its electronic properties can influence the transistor's operation and overall device performance.
Overall, 2,6-Diphenylbenzo[1,2-b:4,5-b']difuran's unique structure and properties position it as a versatile compound with a broad range of potential applications in the advancement of organic semiconductor materials and related technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 5379-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5379-77:
(6*5)+(5*3)+(4*7)+(3*9)+(2*7)+(1*7)=121
121 % 10 = 1
So 5379-77-1 is a valid CAS Registry Number.

5379-77-1SDS

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 2,6-Diphenylbenzo[1,2-b:4,5-b']difuran

1.2 Other means of identification

Product number -
Other names 2-Bromothiazole-5-carboxylic Acid Ethyl Ester

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:5379-77-1 SDS

5379-77-1Downstream Products

5379-77-1Relevant academic research and scientific papers

Synthesis and properties of 2,3,6,7-tetraarylbenzo[1,2-b:4,5-b′] difurans as hole-transporting material

Tsuji, Hayato,Mitsui, Chikahiko,Ilies, Laurean,Sato, Yoshiharu,Nakamura, Eiichi

, p. 11902 - 11903 (2008/03/27)

A new zinc-based annulation method produced regioselectively a variety of 2,3,6,7-tetraarylbenzo[1,2-b:4,5-b′]difurans in good yields. The organic electroluminescent devices using these tetraarylbenzodifurans as hole-transporting materials showed better p

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