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α-Tosylamino-β-(4-amidinophenyl)ethyl-chlormethylketonhydroiodid is a complex organic compound with the chemical formula C22H23Cl2IN4O2S. It is a derivative of chlormethylketones, featuring a tosylamino group (TosNH-), a 4-amidinophenyl group, and a chloromethylketone moiety. α-Tosylamino-β-(4-amidinophenyl)ethyl-chlormethylketonhydroiodid is known for its reactivity and is often used in peptide synthesis as a protecting group or as a reagent to modify peptides and proteins. Its structure allows for specific interactions with amino acid side chains, making it a valuable tool in biochemistry and medicinal chemistry for the development of new drugs and the study of protein function.

88910-10-5

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88910-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88910-10-5 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 88910-10:
(7*8)+(6*8)+(5*9)+(4*1)+(3*0)+(2*1)+(1*0)=155
155 % 10 = 5
So 88910-10-5 is a valid CAS Registry Number.

88910-10-5Downstream Products

88910-10-5Relevant 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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