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α-(1-Naphthylsulfonylamino)-β-(4-amidinophenyl)ethyl-chlormethylketonhydroiodid is a complex organic compound with the chemical formula C22H21Cl2HI2N5O2S. It is a derivative of chlormethylketones, featuring a naphthylsulfonylamino group at the α-position and an amidinophenyl group at the β-position. α-(1-Naphthylsulfonylamino)-β-(4-amidinophenyl)ethyl-chlormethylketonhydroiodid is known for its potential applications in chemical research and as a reagent in various synthetic processes. Its structure includes a chloromethylketone moiety, which is a key functional group in many organic reactions, and the presence of the hydroiodide salt suggests it may be used in conditions where the ionic form is beneficial. The compound's specific properties and reactivity make it a valuable tool in the synthesis of pharmaceuticals and other specialty chemicals.

88910-11-6

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88910-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88910-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,1 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88910-11:
(7*8)+(6*8)+(5*9)+(4*1)+(3*0)+(2*1)+(1*1)=156
156 % 10 = 6
So 88910-11-6 is a valid CAS Registry Number.

88910-11-6Downstream Products

88910-11-6Relevant academic research and scientific papers

Synthetic serine protease inhibitors. 29. Synthesis of alpha-arylsulphonylamino-beta-(4-amidinophenyl)ethyl-chloromethylketones and their inhibitory activity against trypsin, plasmin and thrombin

Horn,Wagner,Stuerzebecher,Walsmann,Markwardt

, p. 581 - 584 (2007/10/02)

The synthesis of alpha-arylsulphonylamino-beta-(4-amidinophenyl)ethyl-chloromethylketones, the structures of which correspond largely to those of the antiproteolytically very potent N alpha-arylsulphonylated 4-amidinophenylalaninamides, was realized start

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