37097-17-9

Basic information

• Product Name: 14-(p-hydroxyphenyl)-14H-dibenzo[a,j]xanthene
• Synonyms: 14-(p-hydroxyphenyl)-14H-dibenzo[a,j]xanthene
• CAS NO: 37097-17-9
• Molecular Weight: 374.439
• Mol File: 37097-17-9.mol

Chemical Properties

• CAS DataBase Reference: 14-(p-hydroxyphenyl)-14H-dibenzo[a,j]xanthene(CAS DataBase Reference)
• NIST Chemistry Reference: 14-(p-hydroxyphenyl)-14H-dibenzo[a,j]xanthene(37097-17-9)
• EPA Substance Registry System: 14-(p-hydroxyphenyl)-14H-dibenzo[a,j]xanthene(37097-17-9)

Safety Data

• Hazardous Substances Data: 37097-17-9(Hazardous Substances Data)

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 135-19-3 β-naphthol 
• 16435-03-3 4-((2-phenylhydrazono)methyl)phenol 
• 93-09-4 naphthalene-2-carboxylate 

Relevant articles and documents

Solvent-free synthesis of 14-aryl-14H-dibenzo[a-j]xanthenes using Fe3O4@Al2O3@SiO2@Fe2O3 as a green catalyst

We report, a novel, green, nano-sized particles as a sandwich nano-capsule multilayer catalyst (SNC@MC) [Fe3O4@Al2O3@SiO2@Fe2O3] for the efficacious one-pot synthesis of 14-aryl-

Alkene-modified Fe3O4 nanoparticle-mediated construction of functionalized mesoporous poly(ionic liquid)s: Synergistic catalysis of mesoporous confinement effect and hydrogen proton for organic transformations

The preparation of mesoporous poly(ionic liquid)s (MPILs) is critically fundamental for the design of heterogeneous catalysts, whereas traditional methods are difficult to obtain these materials with both well-defined mesoporous structure and unique functionality. Here, HClO4-functionalized MPILs with well-defined mesoporous structure were successfully fabricated, in which the alkene-modified Fe3O4 nanoparticles as structural reinforcer play a vital role for mesoporous structure formation. The MPILs were characterized by N2 adsorption/desorption, scanning electron microscope (SEM), transmission Electron Microscope (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and vibration sample magnetometry (VSM), and the results confirm that MPILs possess moderate surface area, well-defined mesoporosity, abundant active ionic centers, as well as efficient magnetic recovery. The resulting MPILs show excellent catalytic activity for condensation reaction and Knoevenagel condensation. The kinetic study reveals that the excellent catalytic activity of MPILs is attributed to the synergistic catalysis of mesoporous confinement effect and hydrogen proton from MPILs, albeit with mass transfer resistance produced by mesoporous channels. Further, the catalyst can be recovered using an external magnetic field and reused at least 10 times without a considerable decrease in its catalytic activity. Finally, alkene-modified Fe3O4 nanoparticle-mediated mesoporous construction promotes a textural engineering approach to the development of novel mesoporous materials for other applications.

A rapid and quantitative synthesis of xanthene derivatives using sulfonated graphitic carbon nitride under ball‐milling

A truly green, solventless, and fast protocol for the quantitative preparation of biologically active xanthene derivatives with 10 mol% sulfonated graphitic carbon nitride (Sg─CN) as a heterogeneous acidic catalyst was developed. Excellent yields, low cost, solvent‐free conditions, high catalytic activity, reusability of the catalyst, simple workup, and heterogeneous carbon‐based catalyst make the present method particularly attractive from a green chemistry perspective.

Sulfamic acid functionalized 3D-network nanoporous polymer based on calix[4]resorcinarene: a recyclable heterogeneous nanocatalyst for the efficient synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes under thermal neat conditions

Abstract: The new synthesized sulfamic acid functionalized catalyst on the basis of calix[4]resorcinarene catalyzed successfully and efficiently the synthesis of 14-aryl-14H-dibenzo[a,j]xanthene derivatives through a one-pot condensation reaction of β-nap

Nano nickel-cobalt ferrite catalyzed one pot synthesis of 14-Aryl-14H-dibenzo[a, j]xanthenes and 12-Aryl-8, 9, 10, 12-tetrahydrobenzo[a]xanthene-11-one derivatives

A simple, green and multi component, one pot synthesis of 14-Aryl-14H-dibenzo[a, j]xanthene derivatives by condensation of aryl aldehydes with 2-naphthol using magnetically separable and recyclable heterogeneous catalyst nano nickel cobalt ferrite (Nisub

Sulfonated starch nanoparticles: An effective, heterogeneous and bio-based catalyst for synthesis of 14-aryl-14-H-dibenzo[a,j]xanthenes

In recent years, biodegradable polymer based nanoparticles have attracted wide attention for the synthesis of high-performance and green catalytic species. Polymeric nanoparticles used for catalytic processes must be biocompatible and biodegradable. The o

Metal free Lewis acid promoted one-pot synthesis of 14-aryl-14H dibenzo [a,j] xanthenes and their simple biological evolution

A green, competent one-pot synthesis of 14-aryl 14H-dibenzo [a,j] xanthene and its bio-computational studies are reported. Target compounds are prepared by the condensation of 2-naphthol with benzaldehyde and its substituents using metal free benzyltrimet

Ruthenium anchored on multi-walled carbon nanotubes: an efficient and reusable catalyst for the synthesis of xanthenes

A novel and highly efficient ruthenium-based catalyst was synthesized by immobilizing Ru(CO)4 onto functionalized multi-walled carbon nanotubes. The catalyst was characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray analysis, diffuse reflectance UV–Vis spectrophotometry, inductively coupled plasma and elemental analysis. This heterogeneous catalyst was successfully applied in the multi-component synthesis of various xanthene derivatives in good to excellent yields (28 samples, up to 96?% yield) under reflux condition and ultrasonic irradiation. The prepared catalyst was recovered four times without appreciable loss of activity.