124337-34-4 Usage
Description
9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is a chemical compound that features a carbazole core with a benzotriazol-1-ylmethyl group attached to it. This structure endows the molecule with unique photophysical and electronic properties, making it suitable for various applications in the field of materials science and electronics.
Uses
Used in Photoconductor Applications:
9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is used as a component in carbazole-containing charge transport layer photoconductors. Its incorporation enhances the charge transport properties of the photoconductor, which is crucial for the performance of devices such as copiers, laser printers, and electrophotographic imaging systems.
Used in Electronics Industry:
In the electronics industry, 9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is used as a material for the development of advanced photoconductive materials. Its application in this field is driven by the need for improved efficiency and performance in electronic devices, particularly those that rely on photoconductive properties for their operation.
Used in Research and Development:
9-(1H-Benzotriazol-1-ylmethyl)-9H-carbazole is also utilized in research and development settings, where it serves as a starting material or a building block for the synthesis of novel compounds with potential applications in various fields, including optoelectronics, photovoltaics, and molecular electronics. Its unique structure allows for the exploration of new chemical and physical properties, contributing to the advancement of materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 124337-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,3 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124337-34:
(8*1)+(7*2)+(6*4)+(5*3)+(4*3)+(3*7)+(2*3)+(1*4)=104
104 % 10 = 4
So 124337-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H14N4/c1-4-10-17-14(7-1)15-8-2-5-11-18(15)22(17)13-23-19-12-6-3-9-16(19)20-21-23/h1-12H,13H2
124337-34-4Relevant articles and documents
Synthesis of 5,6-Dihydro-4H-pyrido[3,2,1-jk]carbazole via intermolecular [4+2] cycloaddition
Katritzky, Alan R.,Zhang, Guifen,Qi, Ming,Xie, Linghong
, p. 6959 - 6960 (1997)
4-, 4,5- and 4,6-Substituted 5,6-dihydro-4H-pyrido[3,2,1-jk]carbazole are synthesized regioselectively from carbazole by a novel, two step sequence.
Preparation, Lithiation and Transformation of N-(Benzotriazol-1-ylmethyl) Heterocycles
Katritzky, Alan R.,Drewniak-Deyrup, Malgorzata,Lan, Xiangfu,Brunner, Frederic
, p. 829 - 836 (2007/10/02)
Indole, carbazole, pyrrole, imidazole, benzimidazole, 2-methyl- and 2-phenylbenzimidazole, and 1,2,4-triazole have each been converted into their N-(benzotriazol-1-ylmethyl) derivatives.The pyrrole, indole, and carbazole adducts undergo smooth lithiation
