209592-66-5 Usage
Uses
Used in Organic Semiconductors:
2-(2,4-Difluorophenyl)thiophene is used as a building block for the synthesis of organic semiconductors, which are essential components in electronic devices such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic photovoltaics (OPVs). Its unique electronic properties contribute to the performance and efficiency of these devices.
Used in Polymers:
In the polymer industry, 2-(2,4-Difluorophenyl)thiophene is used as a monomer or building block for the synthesis of various polymers with specific properties. These polymers can be tailored for use in different applications, such as in coatings, adhesives, or as components in composite materials.
Used in Pharmaceuticals:
2-(2,4-Difluorophenyl)thiophene is also used in the pharmaceutical industry as a key intermediate in the synthesis of various drug molecules. Its unique structural properties make it a valuable component in the development of new pharmaceuticals with potential therapeutic applications.
Used in Organic Chemistry and Material Science:
Due to its versatile chemical structure and properties, 2-(2,4-Difluorophenyl)thiophene is a valuable component in the field of organic chemistry and material science. It can be used in the synthesis of a wide range of organic materials with diverse applications, making it an important building block for researchers and chemists working in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 209592-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,5,9 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 209592-66:
(8*2)+(7*0)+(6*9)+(5*5)+(4*9)+(3*2)+(2*6)+(1*6)=155
155 % 10 = 5
So 209592-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H6F2S/c11-7-3-4-8(9(12)6-7)10-2-1-5-13-10/h1-6H
209592-66-5Relevant academic research and scientific papers
Flexible routes to thiophenes
Jullien, Helene,Quiclet-Sire, Beatrice,Tetart, Thomas,Zard, Samir Z.
supporting information, p. 302 - 305 (2014/01/23)
Three convergent routes to thiophenes are described, hinging on the radical addition of α-xanthyl ketones to ethyl vinyl sulfide or to vinyl pivalate. The latter route ultimately proved to be the most versatile and efficient (61-94%).
Piperazine compounds as inhibitors of MMP or TNF
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, (2008/06/13)
A compound of formula (I) wherein A is a sulfonyl or a carbonyl; R1is an optionally substituted aryl, an optionally substituted heterocyclic group, an optionally substituted lower alkyl or an optionally substituted lower alkenyl; R2is a hydrogen, an optionally substituted lower alkyl, an optionally substituted aryl or an optionally substituted heterocyclic group; R3is an optionally substituted lower alkyl, an optionally substituted lower alkoxy, an optionally substituted aryloxy, an optionally substitued lower alkenyl, an optionally substituted aryl, an optionally substituted heterocyclic group or an optionally substitued amino; R4is a hydrogen, an optionally substituted lower alkyl, an optionally substituted aryl or an optionally substituted heterocyclic group; R5is a hydrogen, an optionally substituted lower alkyl, an optionally substituted aryl or an optionally substituted heterocyclic group; and R10is a hydroxy or a protected hydroxy, and a pharmaceutically acceptable salt thereof. The compound of the present invention is useful as a medicament for prophylactic and therapeutic treatment of MMP- or TNFα-mediated diseases.
