1445416-81-8 Usage
Chemical class
2-(N-phenyl-2-carbazolyl)benzothiazole belongs to the class of benzothiazole derivatives.
Common uses
It is commonly used as a fluorescent material in organic light-emitting diodes (OLEDs) and as a sensitizer in dye-sensitized solar cells.
Stability and efficiency
2-(N-phenyl-2-carbazolyl)benzothiazole exhibits good stability and high efficiency in organic electronic devices.
Medical and pharmaceutical potential
It has been studied for its potential application in medical and pharmaceutical fields, particularly in cancer therapy and imaging due to its fluorescence properties.
Corrosion inhibition
The compound has shown promising performance as a corrosion inhibitor in metal coatings.
Photoinitiator in photopolymerization
2-(N-phenyl-2-carbazolyl)benzothiazole also serves as a photoinitiator in photopolymerization processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1445416-81-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,4,1 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1445416-81:
(9*1)+(8*4)+(7*4)+(6*5)+(5*4)+(4*1)+(3*6)+(2*8)+(1*1)=158
158 % 10 = 8
So 1445416-81-8 is a valid CAS Registry Number.
1445416-81-8Relevant articles and documents
Iridium complexes containing 2-aryl-benzothiazole ligands: Color tuning and application in high-performance organic light-emitting diodes
Li, Jiuyan,Wang, Renjie,Yang, Ruixia,Zhou, Wei,Wang, Xin
, p. 4171 - 4179 (2013)
Three 2-aryl-benzothiazole chromophores were designed and synthesized for use as major cyclometalating ligands of iridium complexes, in which the aryl groups were N-phenyl-3-carbazolyl, 2-(9,9-dioctyl)fluorenyl and N-phenyl-2-carbazolyl. The homoleptic tris-cyclometalated and heteroleptic bis-cyclometalated iridium complexes, 1-5, were synthesized using these ligands. By adjusting the chemical structures and then the electronic state of these complexes, we were able to continuously tune the phosphorescence from yellow to saturated red with peak wavelengths in the order of 1 -1, 48.2 lm W-1, and 23.0% with CIE (0.46, 0.53), which represent the highest efficiencies for yellow OLEDs up to now. Furthermore, 1 was used to fabricate two-element white OLEDs in combination with a blue phosphor and high efficiencies of 57.9 cd A-1 and 21.9% were achieved, which are among the best efficiencies for two-emitting-component white OLEDs reported so far. The Royal Society of Chemistry 2013.
