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14-(2-nitrophenyl)-14H-dibenzo[a,j]xanthene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66596-10-9

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66596-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66596-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,9 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66596-10:
(7*6)+(6*6)+(5*5)+(4*9)+(3*6)+(2*1)+(1*0)=159
159 % 10 = 9
So 66596-10-9 is a valid CAS Registry Number.

66596-10-9Downstream Products

66596-10-9Relevant academic research and scientific papers

Facile catalyzed preparation of 14-aryl- or alkyl-14-H-dibenzo[a,j] xanthenes by dodecylphosphonic acid and dodecylsulfamic acid: Environmentally benign methods

Ghassamipour, Soheila,Sardarian, Ali Reza

, p. 669 - 674 (2012)

Under mild- and solvent-free conditions, one-pot preparation of 14-alkyl- or 14-aryl-14-H-dibenzo[a,j]xanthenes could proceed in the presence of catalytic amounts of dodecylphosphonic acid (DPA) and dodecylsulfamic acid (DSA) in good to excellent yields.

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

Darya, Naghmeh,Tajik, Hassan

supporting information, p. 3546 - 3564 (2021/11/04)

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

Liu, Zhong-Qiu,Li, Sheng-Nan,Zeng, Qing-Shuai,Liu, Yu-Jing,You, Jin-Mao,Ying, An-Guo

, (2021/02/21)

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.

Fabrication of activated carbon sulfuric acid as an excellent and novel solid acid catalyst, evaluating its catalytic activity in synthesizing 1,8-dioxo-octahydroxanthenes and 14-aryl-14H-dibenzo[a,j]xanthenes

Marandi, Alireza,Koukabi, Nadiya,Zolfigol, Mohammad Ali

, p. 3145 - 3163 (2021/05/03)

In this work, for the first time, a novel and innovative procedure has been utilized to chemically functionalize activated carbon (AC) based on the sulfonation reaction, which can be used in catalytic reactions as a strong solid acid. For this aim, AC mus

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

Azizi, Najmedin,Ghaffarzadeh, Mohammad,Qareaghaj, Omid Hosseinchi

, (2021/07/02)

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.

Br?nsted Acidic Ionic Liquid-Catalyzed Synthesis of 14-Aryl-14H-dibenzo[a,j]xanthenes with Controlled Microwave Heating under Solvent-Free Conditions

Huynh, C. C.,Le, T. N.,Tran, P. H.

, p. 504 - 508 (2020/04/29)

Abstract: 1-Methyl-3-sulfo-1H-imidazol-3-ium chloride([Msim]Cl) catalyzed the condensation of β-naphthol with aromatic aldehydesunder microwave irradiation. This method is efficient to synthesizedibenzoxanthene derivatives in excellent yields, and the cat

Novel ionic liquid [Et3N-SO3H][MeSo3]: Synthesis, characterization and catalytic performance for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes

Sadeghi-Takallo, Masoud,Zare, Abdolkarim

, p. 69 - 76 (2019/03/21)

The main aim of this work is introducing a novel protic acidic ionic-liquid catalyst for organic synthesis. Thus, N,N-diethyl-N-sulfoethanaminium methanesulfonate ([Et3N-SO3H][MeSO3]) was synthesized by the reaction of triethylamine with chlorosulfonic ac

Rapid, efficient and solvent-free synthesis of (un)symmetrical xanthenes catalyzed by recyclable sulfated polyborate

Patil, Manisha S.,Palav, Amey V.,Khatri, Chetan K.,Chaturbhuj, Ganesh U.

supporting information, p. 2859 - 2864 (2017/06/27)

The present study describes a rapid, simple and straightforward approach to the synthesis of 1,8-dioxo-octahydroxanthenes, 14-phenyl-14H-dibenzo[a,j]xanthene and tetrahydrobenzoxanthene-11-ones under solvent-free conditions using sulfated polyborate as a

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

Kusampally, Uppalaiah,Pagadala, Ramakanth,Kamatala, Chinna Rajanna

, p. 3316 - 3318 (2017/07/27)

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

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