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1-(benzylsulfonyl)anthracene-9,10-dione is a complex organic chemical compound with the molecular formula C21H14O3S. It is characterized by an anthracene core, which is a tricyclic aromatic hydrocarbon, and a benzylsulfonyl group attached to the 1-position of the anthracene. The compound features two carbonyl groups at the 9,10-positions, which contribute to its reactivity and potential applications in chemical synthesis. 1-(benzylsulfonyl)anthracene-9,10-dione may be used as an intermediate in the synthesis of various organic compounds, particularly those involving anthracene derivatives, and could have applications in the fields of pharmaceuticals, dyes, or materials science.

2687-62-9

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2687-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2687-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2687-62:
(6*2)+(5*6)+(4*8)+(3*7)+(2*6)+(1*2)=109
109 % 10 = 9
So 2687-62-9 is a valid CAS Registry Number.

2687-62-9Downstream Products

2687-62-9Relevant academic research and scientific papers

Carbon nanotube-ruthenium hybrid towards mild oxidation of sulfides to sulfones: Efficient synthesis of diverse sulfonyl compounds

Almeida, Renata G.,De Carvalho, Renato L.,Nunes, Mateus P.,Gomes, Roberto S.,Pedrosa, Leandro F.,De Simone, Carlos A.,Gopi, Elumalai,Geertsen, Valérie,Gravel, Edmond,Doris, Eric,Da Silva Júnior, Eufranio N.

, p. 2742 - 2748 (2019/06/17)

A heterogeneous catalyst was assembled with ruthenium nanoparticles on carbon nanotubes and used in a mild oxidation method to prepare sulfones from sulfides. The system proved very efficient on the investigated substrates and the products were obtained in high yields.

Direct sequential C-H iodination/organoyl-thiolation for the benzenoid A-ring modification of quinonoid deactivated systems: A new protocol for potent trypanocidal quinones

Jardim, Guilherme A. M.,Oliveira, Willian X. C.,De Freitas, Rossimiriam P.,Menna-Barreto, Rubem F. S.,Silva, Thaissa L.,Goulart, Marilia O. F.,Da Silva Júnior, Eufranio N.

supporting information, p. 1686 - 1691 (2018/03/21)

We report a sequential C-H iodination/organoyl-thiolation of naphthoquinones and their relevant trypanocidal activity. Under a combination of AgSR with a copper source, sulfur-substituted benzenoid quinones were prepared in high yields (generally >90%). This provides an efficient and general method for preparing A-ring modified naphthoquinoidal systems, recognized as a challenge in quinone chemistry.

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