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N-(1-phenyl-1H-pyrazol-3-yl)benzenesulfonamide is a chemical compound with the molecular formula C17H14N3O2S. It is a derivative of benzenesulfonamide, featuring a phenylpyrazole moiety attached to the nitrogen atom. N-(1-phenyl-1H-pyrazol-3-yl)benzenesulfonamide is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block for the synthesis of various biologically active molecules. Its structure combines the properties of both benzene and pyrazole rings, which can contribute to its reactivity and interaction with biological targets. The compound's specific role in these applications is determined by its ability to form hydrogen bonds and its potential to act as a ligand in coordination chemistry.

2589-99-3

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2589-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2589-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2589-99:
(6*2)+(5*5)+(4*8)+(3*9)+(2*9)+(1*9)=123
123 % 10 = 3
So 2589-99-3 is a valid CAS Registry Number.

2589-99-3Downstream Products

2589-99-3Relevant academic research and scientific papers

Sulfonamidation of Aryl and Heteroaryl Halides through Photosensitized Nickel Catalysis

Kim, Taehoon,McCarver, Stefan J.,Lee, Chulbom,MacMillan, David W. C.

supporting information, p. 3488 - 3492 (2018/03/05)

Herein we report a highly efficient method for nickel-catalyzed C?N bond formation between sulfonamides and aryl electrophiles. This technology provides generic access to a broad range of N-aryl and N-heteroaryl sulfonamide motifs, which are widely represented in drug discovery. Initial mechanistic studies suggest an energy-transfer mechanism wherein C?N bond reductive elimination occurs from a triplet excited NiII complex. Late-stage sulfonamidation in the synthesis of a pharmacologically relevant structure is also demonstrated.

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