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Benzene, 1-fluoro-4-[(4-nitrophenyl)sulfonyl]-, also known as 4-fluorobenzenesulfonyl chloride or 4-fluorobenzenesulfonic anhydride, is an organic compound with the chemical formula C12H8ClFNO4S. It is a derivative of benzene, featuring a fluorine atom at the 1-position, a sulfonyl group at the 4-position, and a nitro group attached to the phenyl ring of the sulfonyl group. Benzene, 1-fluoro-4-[(4-nitrophenyl)sulfonyl]- is a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and functional group versatility. It is typically used in the preparation of sulfonamide derivatives and other sulfur-containing compounds, and its properties include high reactivity, thermal stability, and solubility in organic solvents.

383-24-4

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383-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 383-24-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 383-24:
(5*3)+(4*8)+(3*3)+(2*2)+(1*4)=64
64 % 10 = 4
So 383-24-4 is a valid CAS Registry Number.

383-24-4Relevant academic research and scientific papers

Method for synthesizing sulfone compounds under photocatalysis condition

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Paragraph 0139-0143, (2021/03/31)

The invention belongs to the technical field of compound preparation, and particularly relates to a method for synthesizing sulfone compounds under a photocatalysis condition. Aromatic hydrazine and sulfinate are used as raw materials, and under the action of alkali and a solvent, a sulfone compound is generated through reaction under the condition of air or oxygen under the illumination of visible light. According to the method disclosed by the invention, aryl hydrazine is used as an arylation reagent, polyacid salt is used as a catalyst or an organic photosensitizer is used as a catalyst, and the sulfones compound can be efficiently synthesized by coupling with sulfinate under the condition of room temperature through visible light irradiation. The method has good substrate universalityand relatively mild reaction conditions, is not only a substitute for synthesizing sulfone compounds by coupling from simple substrates reported at present, but also broadens the new application of the polyacid salt in the field of photocatalysis.

Mo(VI) complex catalysed synthesis of sulfonees and their modification for anti-HIV activities

Madduluri, Vimal Kumar,Baig, Noorullah,Chander, Subhash,Murugesan, Sankaranarayanan,Sah, Ajay K.

, (2020/01/23)

An efficient method for the synthesis of sulfones has been developed using sugar derived cis-dioxo molybdenum(VI) complex as catalyst and urea hydrogen peroxide as oxygen source. Present method is highly specific for sulfide oxidation irrespective of presence of alkene and aldehyde groups in the same molecule. Synthesis of fifteen sulfones have been reported with 82–98% isolated yields and the catalyst has been reused five times without any loss in its activity. 2-(Phenylsulfonyl)aniline has been condensed with eight different aromatic aldehydes and the products are being explored for HIV-1 reverse transcriptase inhibition activities.

Copper-mediated cascade synthesis of diaryl sulfones via the sandmeyer reaction

Yang, Xiaobo,Shi, Liangliang,Fu, Hua

supporting information, p. 847 - 852 (2014/04/17)

A convenient and efficient method for the copper-mediated cascade synthesis of diaryl sulfones via the Sandmeyer reaction has been developed. The protocol uses readily available aryl amines and arylsulfinic acids as the starting materials, isoamyl nitrite as the diazotizating reagent of the aryl amines, and the method shows mild reaction conditions and high tolerance towards various functional groups in the substrates. Georg Thieme Verlag Stuttgart New York.

1,2,3,4,5,6-HEXAHYDROAZEPINO[4,5-B]INDOLES CONTAINING ARYLSULFONES AT THE 9-POSITION

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Page 16-17, (2010/02/09)

The present invention discloses radioligands of 9-arylsulfone of the formula (I), or a pharmaceutically acceptable salt or enantiomer thereof, which are useful in diagnosing depression, obesity and other CNS disorders.

Preparation process of fluorine substituted aromatic compound

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, (2008/06/13)

A preparation process of a fluorine substituted aromatic compound comprising reacting an alkali metal or alkali earth metal salt of an aromatic compound having a hydroxy group with an organic fluorinating agent is disclosed. As a representative fluorinating agent, a bis-dialkylamino-difluoromethane compound, for example, 2,2′-difluoro-1,3-dimethylimidazolidine, is exemplified. According to the process, an industrially useful fluorinated aromatic compound, for example, a fluorobenzene, a fluorine substituted benzophenone, a fluorine substituted diarylsulfone can be prepared with ease in economy without specific equipment.

Potential antileprotic agents. I. Inhibition of a model mycobacterial system by diaryl sulfones

Colwell,Chan,Brown,DeGraw,Peters,Morrison

, p. 142 - 144 (2007/10/12)

The development of a new antileprotic agent poses particular problems in view of the fact that the etiological agent of human leprosy, Mycobacterium leprae, cannot be cultured in bacteriological media. However, a correlation has been observed between mini

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