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2-amino-5-chloro-N-propylbenzensulfonamide is a chemical compound with the molecular formula C9H12ClN2O2S. It is an organic molecule that features a benzene ring with a sulfonamide group attached to it. The sulfonamide group is characterized by the presence of a sulfur atom bonded to both an amino group and an alkyl group, in this case, a propyl chain. The compound also has a chlorine atom at the 5-position of the benzene ring and an amino group at the 2-position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. It is important to note that the handling and use of 2-amino-5-chloro-N-propylbenzensulfonamide should be done with caution, as sulfonamides can have various biological activities and may require specific safety measures during their manipulation.

5790-86-3

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5790-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5790-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5790-86:
(6*5)+(5*7)+(4*9)+(3*0)+(2*8)+(1*6)=123
123 % 10 = 3
So 5790-86-3 is a valid CAS Registry Number.

5790-86-3Upstream product

5790-86-3Downstream Products

5790-86-3Relevant academic research and scientific papers

A novel class of allosteric modulators of AMPA/Kainate receptors

Cannazza, Giuseppe,Jozwiak, Krzysztof,Parenti, Carlo,Braghiroli, Daniela,Carrozzo, Marina M.,Puia, Giulia,Losi, Gabriele,Baraldi, Mario,Lindner, Wolfgang,Wainer, Irving W.

, p. 1254 - 1257 (2009)

The rapid hydrolysis in vivo of IDRA21 to 2-amino-5-chlorobenzensulfonamide has been demonstrated by microdialysis experiments. The IDRA21 metabolite possess in vitro a biological activity similar to that of IDRA21 itself. Taking 2-amino-5-chlorobenzensulfonamide as lead compound, a novel class of AMPAR positive allosteric modulators has been prepared.

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