893736-91-9 Usage
Uses
Used in Organic Electronics Industry:
2,3'-bithiophene-5'-carbaldehyde is used as a key component in the synthesis of organic electronic materials due to its distinctive electronic properties and structural characteristics. It serves as a crucial building block for creating innovative materials with potential applications in various electronic devices.
Used in Organic Light-Emitting Diodes (OLEDs):
In the field of OLEDs, 2,3'-bithiophene-5'-carbaldehyde is utilized as a material for the development of light-emitting layers. Its properties contribute to the efficiency and performance of OLEDs, making it a valuable component in the design and fabrication of these devices.
Used in Organic Photovoltaics (OPVs):
2,3'-bithiophene-5'-carbaldehyde is employed as a material in the construction of organic photovoltaic cells. Its role in these devices is to enhance the light absorption and charge transport properties, which are essential for improving the overall efficiency and performance of OPVs.
Used in Optoelectronic Devices:
Beyond OLEDs and OPVs, 2,3'-bithiophene-5'-carbaldehyde is also used in other optoelectronic devices. Its electronic properties make it suitable for applications where the manipulation of light and its interaction with electronic components is necessary, such as in sensors, communication devices, and imaging systems.
Check Digit Verification of cas no
The CAS Registry Mumber 893736-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,7,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 893736-91:
(8*8)+(7*9)+(6*3)+(5*7)+(4*3)+(3*6)+(2*9)+(1*1)=229
229 % 10 = 9
So 893736-91-9 is a valid CAS Registry Number.
893736-91-9Relevant academic research and scientific papers
INHIBITORS TARGETING DRUG-RESISTANT INFLUENZA A
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Paragraph 0380, (2013/06/27)
Provided are compounds according to formula (la) or (lb) as described herein, that are capable of modulating the activity of influenza viruses (e.g., influenza A virus), for example, via interaction with the M2 transmembrane protein, and other similar viroporins. Also provided are methods for treating an influenza A-affected disease state or infection comprising administering a composition comprising one or more compounds according to according to formulas (la') or (lb), as described herein.
Comparative study of new and known thienyl derivatives of ene-yne benzylamine as mammalian squalene epoxidase inhibitors
Gotteland,Junquero,Oms,Delhon,Halazy
, p. 333 - 342 (2007/10/03)
Analogs of the well-known squalene epoxidase inhibitor (SE) NB-598 (2) have been prepared and tested as cholesterol biosynthesis inhibitors in HepG2 cells. Among the compounds tested, the vinylthiophene analog 4 and the tertiary amide derivative of thiophene 8 emerged as potent human SE inhibitors and probably bind to the enzyme in a very similar manner as NB-598 (2). Surprisingly enough, compounds 4 and 8, contrary to NB-598, are poor inhibitors of rat SE, thus further demonstrating major differences between mammalian enzymes from different species.
