24275-95-4

Basic information

• Product Name: 10-(4-bromophenyl)-9(10H)-acridinon
• Synonyms: 10-(4-bromophenyl)-9(10H)-acridinon;10- (4-Bromophenyl) -9 (10H) -acridone
• CAS NO: 24275-95-4
• Molecular Formula: C₁₉H₁₂BrNO
• Molecular Weight: 350.20868
• Mol File: 24275-95-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 278.5-279.5 °C
• Boiling Point: 481.3±34.0 °C(Predicted)
• Appearance: /
• Density: 1.496±0.06 g/cm3(Predicted)
• PKA: -6.23±0.20(Predicted)
• CAS DataBase Reference: 10-(4-bromophenyl)-9(10H)-acridinon(CAS DataBase Reference)
• NIST Chemistry Reference: 10-(4-bromophenyl)-9(10H)-acridinon(24275-95-4)
• EPA Substance Registry System: 10-(4-bromophenyl)-9(10H)-acridinon(24275-95-4)

Safety Data

• Hazardous Substances Data: 24275-95-4(Hazardous Substances Data)

Usage

General Description

10-(4-bromophenyl)-9(10H)-acridinon is a chemical compound that belongs to the acridinone family, and it contains a bromophenyl group. It is a heterocyclic compound with a molecular formula of C19H12BrNO. This chemical has potential applications in pharmaceuticals, as it exhibits various biological activities such as anticancer, antiviral, and antimicrobial properties. Additionally, it is known for its role as a fluorescent dye in bioimaging applications. Its unique structure and properties make it a promising candidate for further research in drug development and medical diagnostics.

Upstream product

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Relevant articles and documents

Compound for organic luminescence and application thereof

The invention relates to a compound for organic luminescence. The structure of the compound is shown as a formula (I) in the description, wherein X is selected from one of carbonyl, oxygen atom or sulfur atom; and the formula (I) is also connected with a

Mechanochromism, Twisted/Folded Structure Determination, and Derivatization of (N-Phenylfluorenylidene)acridane

(N-Phenylfluorenylidene)acridane (Ph-FA) compounds with electron-withdrawing and -donating substituents (H, MeO, Ph, NO2, Br, F) at the para position of the phenyl group were successfully synthesized by Barton–Kellogg reactions of N-aryl thioacridones and diazofluorene. By using the substituent on the nitrogen atom to alter the electronic properties, both the folded and twisted conformers of p-NO2-C6H4-FA could be crystallographically characterized, which enabled the charge transfer from the electron-donating acridane moiety to the electron-accepting fluorenylidene moiety to be understood. Ground-state mechanochromism, thermochromism, vapochromism, and proton-induced chromism were demonstrated between the folded and twisted conformations of the conformers. Protonation and chemical oxidation of Ph-FA gave two stable acridinium compounds, namely, the fluorenylacridinium and acridinium radical cations. The present study will contribute to the development of functional dyes and organic semiconductors.

Copper-catalyzed intramolecular direct amination of sp2 C-H bonds for the synthesis of N-aryl acridones

A copper-catalyzed approach for the synthesis of N-aryl acridones via sp2 C-H bond amination using air as oxidant under neutral conditions is disclosed. This reaction not only provides a complementary method for synthesizing medicinally important acridones, but also offers a new strategy for sp2 C-H bond amination.