51678-15-0

Basic information

• Product Name: 2,5-di-(2'-thienyl)selenophene
• Synonyms: 2,5-di-(2'-thienyl)selenophene
• CAS NO: 51678-15-0
• Molecular Formula: C12H8 S2 Se
• Molecular Weight: 295.28
• Mol File: 51678-15-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-di-(2'-thienyl)selenophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-di-(2'-thienyl)selenophene(51678-15-0)
• EPA Substance Registry System: 2,5-di-(2'-thienyl)selenophene(51678-15-0)

Safety Data

• Hazardous Substances Data: 51678-15-0(Hazardous Substances Data)

Usage

Structure

Selenophene ring with two thienyl substituents The compound is composed of a selenophene ring (a ring with selenium and carbon atoms) and two thienyl groups (containing a sulfur atom and a five-membered carbon ring) attached to it.

Organoselenium compound

Diverse biological and pharmaceutical applications 2,5-di-(2'-thienyl)selenophene belongs to a class of compounds containing selenium, which are known for their various biological and pharmaceutical properties.

Potential semiconductor material

Organic electronics The compound has garnered interest due to its possible use in organic electronics, such as organic photovoltaic cells and field-effect transistors, owing to its unique structural and electronic properties.

Antioxidant and anticancer properties

Medicinal chemistry significance 2,5-di-(2'-thienyl)selenophene has been studied for its potential to act as an antioxidant and exhibit anticancer activity, making it an important compound in the fields of materials science and medicinal chemistry.

Upstream product

• 16900-51-9 1,4-bis(2-thienyl)butadiyne 
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• 5713-61-1 thiophen-2-yl magnesium bromide 
• 4298-52-6 2-ethynyl-thiophene 
• 288-05-1 selenophene 
• 1003-09-4 2-bromothiophene 

Relevant articles and documents

Synthesis f Mixed Oligomeric Heteroarylenes containing Thiophene and Selenophene Rings; their U.V.Spectra and Oxidation Potentials

Mixed oligomers containing thiophene and selenophene rings have been synthesized; their u.v. spectra and oxidation potentials determined and discussed in terms of coplanarity of the rings and the +I-effect of the methyl substituent.

2,5-disubstituted selenophen compound and synthesis method thereof

The invention belongs to the technical field of organic synthesis, and discloses a 2,5-disubstituted selenophen compound and a synthesis method thereof. The synthesis method comprises the following steps: adding an alkynyl-terminated compound, elemental s

SYNTHESIS OF MIXED OLIGOMERIC HETEROARYLENES CONTAINING FURAN, THIOPHENE, AND SELENOPHENE RINGS; THEIR UV SPECTRA AND OXIDATION POTENTIALS

Mixed oligomeric five-membered heteroarylenes 3a-f and 4a-e have been prepared by cross-coupling reaction of the Grignard reagents 2 derived of the appropriately substituted thiophenes 1 with either the 2-bromoheteroarylenes or the 2,5-dibromoheteroarylenes derived of furan, thiophene, and/or selenophene respectively.The UV spectra and oxidation potential of compounds 3a-f and 4a-e are discussed on the basis of co-planarity. Key words; Conducting polymers; oligomeric heteroarylenes; UV spectra; oxidation potentials.