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

58162-87-1

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58162-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58162-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,6 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58162-87:
(7*5)+(6*8)+(5*1)+(4*6)+(3*2)+(2*8)+(1*7)=141
141 % 10 = 1
So 58162-87-1 is a valid CAS Registry Number.

58162-87-1Downstream Products

58162-87-1Relevant academic research and scientific papers

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-

A clean, mild, and efficient preparation of aryl 14H-benzo[a,j]xanthene leuco-dye derivatives via nanocatalytic MCM-41-SO3h under ultrasonic irradiation in aqueous media

Fathollahi, Mostafa,Rostamizadeh, Shahnaz,Amani, Ali M.

, p. 5 - 13 (2018/06/19)

Aim and Objective: The present study has developed an efficient and eco-friendly protocol for the synthesis of aryl-14-H-dibenzo[a,j] xanthenes through a one-pot condensation reaction of 2-naphthol and arylaldehydes in aqueous media using the nanocatalyti

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

Safari, Javad,Aftabi, Pegah,Ahmadzadeh, Majid,Sadeghi, Masoud,Zarnegar, Zohre

, p. 33 - 39 (2017/04/21)

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

Fe+3-montmorillonite K10 as an Efficient Reusable Heterogeneous Catalyst for the Grind Mediated Synthesis of 14-aryl-14H-dibenzo [a,j]xanthenes

Fekri, Leila Z.,Nikpassand, Mohammad,Fard, Hajar S.,Marvi, Omid

, p. 135 - 142 (2016/03/01)

Background: Xanthenes are an important class of organic compounds and have also received significant attention due to their wide range of pharmacological activities such as antibacterial, antiviral, antiinflammatory activities, antagonists for the paralyzing action of zoxazolamine and efficiency in photodynamic therapy, a well-known method for controlling the localized tumors. Natural sources are also rich of xanthene compounds. Popularly known pigments, santalin have been isolated from plant species. Furthermore, these compounds can be emerged as pH-sensitive fluorescent materials for visualization of biomolecules, in laser technologies and as dyes. There are several reports in the literature for the synthesis of xanthenes such as alkylations of heteroatoms, cyclodehydrations, cyclocondensations between 2-hydroxyaromatic aldehydes and 2- tetralone, trapping of benzynes by phenols and intramolecular phenyl-carbonyl coupling reactions of benzaldehydes and acetophenones bearing tethered carbonyl chains in the presence of hexamethylphosphoramide and SmI2. Other methods for the synthesis of xanthenes include the reaction of formamide with β-naphthol, carbon monoxide, and 1- hydroxymethyl-naphthalen-2-ol. Methods: procedure a: A mixture of substituted benzaldehyde, 2-naphtol and Fe+3-montmorillonite K10 was mixed. After completion of the reaction, the product was solved in CHCl3 (3×10 mL) and insoluble catalyst was removed by filtration. The organic phase including the product and chloroform was evaporated under vacuum. The resulting crude material was purified by recrystallization from EtOH to afford pure products. procedure b: A mixture of substituted benzaldehyde, phenylhydrazine and Fe+3-montmorillonite K10 were added to a mortar and the mixture was pulverized with a pestle. After completion of the reaction, 2-naphtol was added to the consulting mixture and pulverized with a pestle. The organic phase including the product and chloroform was evaporated under vacuum. The resulting crude material was purified by recrystallization from EtOH to afford pure products. Results: As part of our going interest for the development of efficient and environmentally friendly procedures for the synthesis of heterocyclic and pharmaceutical compounds, we wish to report the first grind mediated synthesis of some derivatives of xanthenes using catalytic amount of Fe+3-montmotillonite. Conclusion: In conclusion, we have investigated the Fe+3-montmorillonite K10 under grinding as a mild and efficient catalyst for the synthesis of substituted 14-aryl-14H-dibenzo [a,j]xanthenes. The remarkable advantages offered by this method are: catalyst is inexpensive, non-toxic, easy handling and reusability, simple work-up procedure, short reaction time, high yields of product with better purity and green aspect by avoiding toxic catalyst and hazardous solvent.

1,4-Diazaniumbicyclo[2.2.2]octane diacetate: As an effective, new and reusable media for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes

Fekri, Leila Zare,Fard, Hajar Saeedi

, p. 263 - 270 (2016/07/06)

A general synthetic route to dibenzoxanthenes has been developed using 1,4-diazaniumbicyclo[2.2.2]octane diacetate as a new bis ionic liquid under thermal and solvent free condition. This method provides several advantages such as a simple work-up, environmental friendliness and shorter reaction time along with high yields. All of the synthesized compounds were characterized by infrared spectroscopy, 1H and 13C spectroscopy and elemental analyses.

Antimony (III) acetate as a versatile and efficient catalyst for synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes at room temperature

Hakimi, Fatemeh,Hassanabadi, Alireza

, p. 53 - 55 (2015/02/05)

Antimony (III) acetate was used in the one-pot three-component synthesis of biologically active 14-aryl-14H-dibenzo[a,j ] xanthenes from the condensation between arylaldehydes and naphthol under solvent-free conditions at ambient temperature. This methodo

Secondary amine based ionic liquid: An efficient catalyst for solvent free one pot synthesis of xanthenes and benzoxanthenes

Das, Pranab J.,Das, Jupitara

, p. 11745 - 11752 (2015/02/19)

Ionic liquids (IL) prepared from dialkylamines and concentrated sulphuric acid were used in an operationally simple, cost effective, efficient and environmentally benign synthesis of xanthenes and benzoxanthenes. Three ILs were screened for their efficien

Efficient one-pot synthesis of 14-aryl-14H-dibenzo[a,j]xanthene derivatives promoted by niobium pentachloride

De Andrade Bartolomeu, Aloisio,De Menezes, Manoel Lima,De Silva Filho, Luiz Carlos

, p. 1593 - 1600 (2015/03/30)

A simple and efficient procedure for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthene derivatives through one-pot condensation of 2-naphthol with aryl aldehydes in the presence of niobium pentachloride is described. The reactions were carried out using 2

Efficient one-pot synthesis of 14-aryl-14H-dibenzo[a,j]xanthene derivatives promoted by niobium pentachloride

De Andrade Bartolomeu, Aloisio,De Menezes, Manoel Lima,Da Silva Filho, Luiz Carlos

, p. 1593 - 1600 (2015/02/19)

A simple and efficient procedure for the synthesis of 14-aryl-14H-dibenzo[a,j ]xanthene derivatives through one-pot condensation of 2-naphthol with aryl aldehydes in the presence of niobium pentachloride is described. The reactions were carried out using

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