146886-04-6 Usage
Description
(4-HYDROXYANILINO)(IMINO)METHANESULFINIC ACID, also known as N-(4-aminophenyl)methanesulfonamide, is a chemical compound with the formula C7H8N2O3S. It is a sulfonamide derivative known for its unique chemical structure and properties, making it a valuable tool in the pharmaceutical industry and organic synthesis.
Used in Pharmaceutical Industry:
(4-HYDROXYANILINO)(IMINO)METHANESULFINIC ACID is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical properties and potential therapeutic applications.
Used in Antiviral Applications:
(4-HYDROXYANILINO)(IMINO)METHANESULFINIC ACID is used as an antiviral agent for its potential to combat viral infections, offering a promising avenue for the development of new antiviral medications.
Used in Antineoplastic Applications:
(4-HYDROXYANILINO)(IMINO)METHANESULFINIC ACID is used as an antineoplastic agent, indicating its potential role in treating cancer by inhibiting the growth and spread of tumors.
Used in Catalyst Applications:
(4-HYDROXYANILINO)(IMINO)METHANESULFINIC ACID is used as a catalyst in organic synthesis reactions, facilitating various chemical processes and contributing to the development of new drugs and chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 146886-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,8,8 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146886-04:
(8*1)+(7*4)+(6*6)+(5*8)+(4*8)+(3*6)+(2*0)+(1*4)=166
166 % 10 = 6
So 146886-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O3S/c8-7(13(11)12)9-5-1-3-6(10)4-2-5/h1-4,10H,(H2,8,9)(H,11,12)
146886-04-6Relevant articles and documents
Biological properties of amidinium sulfinic and sulfonic acid derivatives: inhibition of glycolytic enzymes of Trypanosoma brucei and protective effect on cell growth
Willson, M,Perie, JJ,Malecaze, F,Opperdoes, F,Callens, M
, p. 799 - 808 (2007/10/02)
The activity of the title compounds has been investigated on two biological targets: cultures of trypanosome and glycolytic enzymes inhibition of the parasite, and on retinal epithelium cells.In both cases, these compounds exhibit a significant activity,
