500286-36-2

Basic information

• Product Name: 9H-Xanthen-9-one, 3-bromo-
• Synonyms: 9H-Xanthen-9-one, 3-bromo- ;3-bromo-9H-xanthen-9-one;3-bromoxanthenon
• CAS NO: 500286-36-2
• Molecular Formula: C₁₃H₇BrO₂
• Molecular Weight: 275.09748
• Mol File: 500286-36-2.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 403.2±34.0 °C(Predicted)
• Appearance: /
• Density: 1.620±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 9H-Xanthen-9-one, 3-bromo-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Xanthen-9-one, 3-bromo-(500286-36-2)
• EPA Substance Registry System: 9H-Xanthen-9-one, 3-bromo-(500286-36-2)

Safety Data

• Hazardous Substances Data: 500286-36-2(Hazardous Substances Data)

Usage

General Description

9H-Xanthen-9-one, 3-bromo- is a chemical compound with the molecular formula C13H9BrO and a molecular weight of 265.11 g/mol. It is a brominated derivative of xanthen-9-one and is commonly used as a fluorescent dye and in the synthesis of organic compounds. 9H-Xanthen-9-one, 3-bromo- is known for its bright red fluorescence under ultraviolet light, making it useful in applications such as fluorescent microscopy, flow cytometry, and bioimaging. It is also used in the production of fluorescent materials, optical brighteners, and various other research and industrial processes. Additionally, 9H-Xanthen-9-one, 3-bromo- has potential applications in the fields of medical diagnostics, drug discovery, and environmental monitoring due to its fluorescent properties.

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Downstream Products

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Relevant articles and documents

Synthesis of xanthones from 4-(2-phenoxyphenyl)-1-tosyl-1H-1,2,3-triazole via rhodium-catalyzed annulation/oxidation

A series of xanthone derivatives were synthesized by rhodium-catalyzed cycloaddition and sequential oxidation. The derivatives synthesized for excellent yields, including electron-withdrawing and electron-donating substituents, demonstrated the wide applicability of the proposed approach. The xanthones synthesized with different substituent electron effects may go through the same intermediate via two cycloadditions. It is highlighted that the protocol was exemplified by its successful integration into a one-pot synthesis directly from 1-ethynyl-2-phenoxybenzene. We believe that the current method may be an attractive option for the synthesis of xanthone and its derivatives.

Anthraquinone general formula compound and application thereof

The invention discloses an anthraquinone general formula compound and application thereof. The general formula compound is shown in a formula in the specification, in the formula, Y represents an oxygen atom or a sulfur atom, X1 to X8 represent C, CR or N

Cu(0)/Selectfluor system-catalyzed intramolecular Csp2-H/Csp2-H cross-dehydrogenative coupling (CDC)

A Cu(0)/Selectfluor system-catalyzed intramolecular Csp2-H/Csp2-H bond cross-dehydrogenative coupling of 2-aryloxybenzaldehydes is described. A variety of substituted xanthone derivatives are synthesized in moderate to excellent yields. Reaction can also be extended to the synthesis of 9H-thioxanthen-9-one 10,10-dioxide and phenanthridin-6(5H)-ones, respectively.