481695-75-4 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bisis utilized as a key intermediate in organic synthesis for the creation of complex organic molecules. Its unique structure allows for multiple points of chemical modification, facilitating the synthesis of novel compounds with tailored properties.
Used in Materials Science:
In the field of materials science, Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bisis employed as a building block for the development of new materials with specific optical, electronic, or mechanical properties. The carbazole moiety's inherent characteristics, such as its planarity and electronic properties, contribute to the performance of these materials.
Used in Pharmaceutical Research:
Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bisserves as a promising candidate in pharmaceutical research for the development of new drugs. The carbazole core is known to exhibit a range of biological activities, and the presence of phenylmethyl substituents may further modulate these properties, leading to the discovery of new therapeutic agents.
Used in Chemical Sensors:
Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bismay also be used in the development of chemical sensors due to the potential for specific interactions with target analytes. The carbazole-based structure could provide selective binding sites, making it suitable for detecting certain chemicals or environmental pollutants.
Used in Dye-synthesis:
Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]biscan be employed in the synthesis of dyes for various applications, including textiles, inks, and pigments. Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bis-'s chromophoric properties and the possibility of tuning its color through structural modifications make it a valuable asset in this industry.
Used in Photoactive Materials:
In the development of photoactive materials, such as solar cells or light-emitting diodes, Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bis- may be utilized for its light-absorbing and light-emitting properties. The carbazole-based structure is known for its ability to participate in charge transfer processes, which is crucial for these applications.
Each of these applications is contingent upon the specific properties that Ethanone, 1,1'-[9-(phenylmethyl)-9H-carbazole-3,6-diyl]bisexhibits, which would be determined through further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 481695-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,6,9 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 481695-75:
(8*4)+(7*8)+(6*1)+(5*6)+(4*9)+(3*5)+(2*7)+(1*5)=194
194 % 10 = 4
So 481695-75-4 is a valid CAS Registry Number.
481695-75-4Relevant academic research and scientific papers
Novel syntheses of carbazole-3,6-dicarboxylate ligands and their utilization for porous coordination cages
Bloch, Eric D.,Rowland, Casey A.,Yap, Glenn P. A.
, p. 16340 - 16347 (2020/12/03)
The molecular nature, and thus potential solubility, of coordination cages endows them with a number of advantages as compared to metal-organic frameworks and other extended network solids. However, their lack of three-dimensional connectivity typically l
Fluorinated tetraketone derivatives of N-substituted carbazoles and their Eu(III) complexes for fluorescence immunoassay
Pugachov, Dmitriy E.,Kostryukova, Tatiana S.,Zatonsky, Georgy V.,Vatsadze, Sergey Z.,Vasil’ev, Nikolai V.
, p. 528 - 534 (2018/07/05)
[Figure not available: see fulltext.] New fluorinated tetraketone derivatives of N-substituted carbazoles were synthesized and tested as ligands for fluorescence immunoassay. The spectral properties of the obtained heterocyclic tetraketones and their Eu(III) complexes were studied. The complexes showed longwave absorption at 360–380 nm, high extinction coefficient values, long lifetime of excited states, and intense luminescence, allowing to consider the use of such lanthanide complexes in immunofluorescence analysis.
