1246308-85-9

Basic information

• Product Name: 12H-benzofuro[3,2-a]carbazole
• Synonyms: 12H-benzofuro[3,2-a]carbazole
• CAS NO: 1246308-85-9
• Molecular Weight: 257.291
• Mol File: 1246308-85-9.mol
• Article Data: 19

Chemical Properties

• Boiling Point: 506.8±23.0 °C(Predicted)
• Density: 1.375±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 12H-benzofuro[3,2-a]carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 12H-benzofuro[3,2-a]carbazole(1246308-85-9)
• EPA Substance Registry System: 12H-benzofuro[3,2-a]carbazole(1246308-85-9)

Safety Data

• Hazardous Substances Data: 1246308-85-9(Hazardous Substances Data)

Usage

Chemical class

Belongs to the benzofuran class of organic compounds.

Structure

A polycyclic aromatic hydrocarbon formed by fusing a benzene and a carbazole ring together with a furan moiety.

Potential carcinogen

12H-benzofuro[3,2-a]carbazole is a potential carcinogen.

Mutagenic properties

It is also a potential mutagen.

Mechanism of action

The exact mechanism of action is not fully understood.

Environmental presence

Detected in environmental samples and considered a possible environmental pollutant.

Human health effects

Studies have shown that exposure to this compound may have adverse effects on human health.

Environmental concern

Its presence in the environment is a cause for concern.

Further research

More research is needed to fully understand its toxicity and potential health risks.

Upstream product

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Relevant articles and documents

Carbazolo-aromatic ring thermal activation delayed fluorescence material and organic electroluminescent device thereof

The invention discloses a carbazolo-aromatic ring thermal activation delayed fluorescence material and an organic electroluminescent device. The structural formula of the carbazolo-aromatic ring thermal activation delayed fluorescent material is shown in the specification. The carbazolo-aromatic ring thermal activation delayed fluorescent material provided by the invention takes a carbazolo-aromatic ring as a core; due to the large volume and rigidity, molecules have a steric hindrance effect, intramolecular distortion is realized, and electron clouds of the highest occupied orbit and the lowest empty orbit of the molecules can be relatively separated to obtain a quite small single triplet state energy level difference, so that light-emitting molecules with a thermal activation delayed fluorescence property are designed and prepared; the thermal performance, the light-emitting efficiency and the light color of the material can be adjusted, and the material can be used as a guest material, can also be used as a host material by utilizing the thermal activation delayed fluorescence property, and can be constructed through molecular design.

Molecular Engineering of Isomeric Benzofurocarbazole Donors for Photophysical Management of Thermally Activated Delayed Fluorescence Emitters

Benzofurocarbazole moieties are commonly used donor structures in the design of thermally activated delayed fluorescence (TADF) emitters. However, only 5 H-benzofuro[3,2-c]carbazole (34BFCz) has been reported and, to the best of our knowledge, no other be

Compound taking cycloheptene as core and application of compound on organic light-emitting devices

The invention discloses a compound taking cycloheptene as a core and an application of the compound on organic light-emitting devices. The compound has strong rigidity due to the cycloheptene structure, and after the compound is connected with a carbazole