What is the 5,11-dihydro-5-phenylindolo[3,2-b]carbazole?

5,11-dihydro-5-phenylindolo[3,2-b]carbazole is , while it's Molecular Formula is C 24 H 16 N 2 . Used in Organic Electronics: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is utilized as a component in organic electronics for its notable electronic and optical properties, which make it suitable for applications such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Used in Biological Research: In the field of biological research, 5,11-dihydro-5-phenylindolo[3,2-b]carbazole serves as a DNA intercalator, a property that allows it to insert itself between the base pairs of DNA, which is useful for studying DNA structure and function. Used in Anti-Cancer Research: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is explored as a potential anti-cancer agent, with ongoing research investigating its ability to target and affect cancer cells, offering a new avenue for cancer treatment development. Used as a Fluorescent Dye: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is also considered for use as a fluorescent dye in various applications, including bioimaging and as a sensor, due to its photophysical properties that allow it to emit light upon excitation. Used in Materials Science: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole's photophysical characteristics make it a candidate for use in materials science, where it could be employed in the development of new materials with specific light absorption, emission, or sensing capabilities.

What is the CAS number for 5,11-dihydro-5-phenylindolo[3,2-b]carbazole?

The CAS number of 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is 1316311-27-9.

What is 5,11-dihydro-5-phenylindolo[3,2-b]carbazole (1316311-27-9) used for?

5,11-dihydro-5-phenylindolo[3,2-b]carbazole is a chemical compound belonging to the carbazole family, characterized by a unique polycyclic aromatic structure that includes a carbazole core, an indole ring, and a phenyl group. 5,11-dihydro-5-phenylindolo[3,2-b]carbazole has garnered interest due to its intriguing electronic and optical properties, as well as its potential biological activities and applications in various scientific fields.

What is the 5,11-dihydro-5-phenylindolo[3,2-b]carbazole?

5,11-dihydro-5-phenylindolo[3,2-b]carbazole is , while it's Molecular Formula is C 24 H 16 N 2 . Used in Organic Electronics: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is utilized as a component in organic electronics for its notable electronic and optical properties, which make it suitable for applications such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Used in Biological Research: In the field of biological research, 5,11-dihydro-5-phenylindolo[3,2-b]carbazole serves as a DNA intercalator, a property that allows it to insert itself between the base pairs of DNA, which is useful for studying DNA structure and function. Used in Anti-Cancer Research: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is explored as a potential anti-cancer agent, with ongoing research investigating its ability to target and affect cancer cells, offering a new avenue for cancer treatment development. Used as a Fluorescent Dye: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is also considered for use as a fluorescent dye in various applications, including bioimaging and as a sensor, due to its photophysical properties that allow it to emit light upon excitation. Used in Materials Science: 5,11-dihydro-5-phenylindolo[3,2-b]carbazole's photophysical characteristics make it a candidate for use in materials science, where it could be employed in the development of new materials with specific light absorption, emission, or sensing capabilities.

What is the CAS number for 5,11-dihydro-5-phenylindolo[3,2-b]carbazole?

The CAS number of 5,11-dihydro-5-phenylindolo[3,2-b]carbazole is 1316311-27-9.

What is 5,11-dihydro-5-phenylindolo[3,2-b]carbazole (1316311-27-9) used for?

5,11-dihydro-5-phenylindolo[3,2-b]carbazole is a chemical compound belonging to the carbazole family, characterized by a unique polycyclic aromatic structure that includes a carbazole core, an indole ring, and a phenyl group. 5,11-dihydro-5-phenylindolo[3,2-b]carbazole has garnered interest due to its intriguing electronic and optical properties, as well as its potential biological activities and applications in various scientific fields.

Product classification

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1316311-27-9

Product Name:5-Phenyl-5,11-dihydroindolo[3,2-b]carbazole
Molecular Weight:332.404

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Product Details

Purity:99%

Factory Supply Industrial Grade 5-Phenyl-5,11-dihydroindolo[3,2-b]carbazole 1316311-27-9 with Best Price

Molecular Formula:C₂₄H₁₆N₂
Molecular Weight:332.404

1316311-27-9 Relevant articles

Organic compound as well as electronic element and device using same

-

Paragraph 0028; 0235-0236; 0258, (2021/05/19)

The invention relates to the technical f...

COMPOUND FOR ORGANIC ELECTRIC ELEMENT AND ORGANIC ELECTRIC DEVICE COMPRISING THE SAME

-

Paragraph 0363-0365; 0368-0369; 0396; 0398; 0401, (2020/11/28)

The present invention relates to a compo...

ORGANIC COMPOUND, MIXTURE COMPRISING SAME, COMPOSITE, AND ORGANIC ELECTRONIC COMPONENT

-

Paragraph 0139; 0140, (2018/05/24)

An organic compound having the following...

To improve the efficiency of thermally activated delayed fluorescence OLEDs by controlling the horizontal orientation through optimizing stereoscopic and linear structures of indolocarbazole isomers

Xiang, Songpo,Lv, Xialei,Sun, Shuaiqiang,Zhang, Qing,Huang, Zhi,Guo, Runda,Gu, Honggang,Liu, Shiyuan,Wang, Lei

, p. 5812 - 5820 (2018/06/07)

Molecular structures play a critical rol...

1316311-27-9 Process route

: 1361125-94-1
2-(2-nitrophenyl)-9-phenyl-9H-carbazole

: 1024598-06-8
11-phenyl-11,12-dihydroindolo[2,3-a]carbazole

: 1316311-27-9
5-phenyl-5,11-dihydro-indolo[3,2-b]carbazole

Conditions

Conditions	Yield
With triphenylphosphine; In 1,2-dichloro-benzene; at 180 ℃; for 24h; Overall yield = 63 %; Inert atmosphere;

: 108-86-1,52753-63-6
bromobenzene

: 6336-32-9
5H,11H-indolo[3,2-b]carbazole

: 1316311-27-9
5-phenyl-5,11-dihydro-indolo[3,2-b]carbazole

Conditions

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; tri-tert-butyl phosphine; sodium t-butanolate; In o-xylene; at 160 ℃; for 48h;	87%
With copper(l) iodide; 18-crown-6 ether; potassium carbonate; In 1,2-dichloro-benzene; at 140 ℃; Inert atmosphere;	3 g

1316311-27-9 Upstream products

5467-74-3
4-Bromophenylboronic acid
35450-34-1
4'-bromo-2-nitrobiphenyl
3652-90-2
2-bromo-9H-carbazole
609-73-4
o-nitroiodobenzene

1316311-27-9 Downstream products

1369587-22-3
C₃₀H₁₉BrN₂
1369587-25-6
C₃₀H₂₁BN₂O₂
1369585-27-2
C₄₈H₃₀N₂

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