13974-79-3 Usage
Uses
Used in Organic Electronics:
N-[(E)-naphthalen-1-ylmethylidene]-9H-fluoren-2-amine is used as a material in the field of organic electronics for its light-emitting properties. It is particularly utilized in the development of light-emitting diodes (LEDs) and organic photovoltaic devices, where its fluorescent characteristics contribute to improved performance and efficiency.
Used in Photodynamic Therapy for Cancer Treatment:
N-[(E)-naphthalen-1-ylmethylidene]-9H-fluoren-2-amine is studied for its potential use as a photosensitizer in photodynamic therapy. Its ability to absorb light and generate reactive oxygen species makes it a candidate for the targeted destruction of cancer cells, offering a non-invasive treatment option for various types of cancer.
Used in Research and Development:
Due to its unique photochemical and photophysical properties, N-[(E)-naphthalen-1-ylmethylidene]-9H-fluoren-2-amine is also used in ongoing research for potential future applications. Scientists are exploring its capabilities in various fields, including materials science, medicinal chemistry, and nanotechnology, to discover new uses and enhance existing technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 13974-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,7 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13974-79:
(7*1)+(6*3)+(5*9)+(4*7)+(3*4)+(2*7)+(1*9)=133
133 % 10 = 3
So 13974-79-3 is a valid CAS Registry Number.
13974-79-3Relevant academic research and scientific papers
Chang, Zhidong,Cheng, Jiapeng,Hu, Tao,Li, Jiaxin,Li, Wenjun,Sun, Changyan,Wang, Lin,Zhao, Yichen
, (2021)
A new fluorescent probe 1-[(9H-fluoren-2-ylimino) methyl]-naphthalene (L) was synthesized which can be used to detect Al3+ and Cr3+ ions by fluorescence enhancement. The detection limits of L for Al3+ and Cr3+ ions were 8.87 × 10-8 and 6.31 × 10-8 M and the coordination constants were 3.25 × 103 and 2.09 × 103, respectively. Job′s plot, 1H NMR titration and mass spectrometry experiments were conducted to discuss the coordination modes and the bonding ratios. The recognition mechanism was that during the recognition process, C[dbnd]N group of L was oxidized into O[dbnd]C-NH and was involved in coordination, which inhibited the C[dbnd]N isomerization and resulted in enhanced fluorescence.
