7409-84-9 Usage
General Description
2-AMINO-5-METHANESULFONYL-BENZENESULFONAMIDE is a chemical compound with the molecular formula C7H10N2O4S2. It is a sulfonamide derivative, which means it contains a sulfur atom bonded to an amino group and a benzene ring. 2-AMINO-5-METHANESULFONYL-BENZENESULFONAMIDE is commonly used as an antimicrobial agent in pharmaceuticals and medical treatments. It works by inhibiting the growth of bacteria through interference with their metabolic processes. Additionally, 2-AMINO-5-METHANESULFONYL-BENZENESULFONAMIDE has been studied for its potential use in treating certain types of cancer, as it has shown promising anti-proliferative and cytotoxic effects on tumor cells. However, it is important to handle 2-AMINO-5-METHANESULFONYL-BENZENESULFONAMIDE carefully, as it can be toxic and harmful if ingested or inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 7409-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7409-84:
(6*7)+(5*4)+(4*0)+(3*9)+(2*8)+(1*4)=109
109 % 10 = 9
So 7409-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O4S2/c1-14(10,11)5-2-3-6(8)7(4-5)15(9,12)13/h2-4H,8H2,1H3,(H2,9,12,13)
7409-84-9Relevant academic research and scientific papers
FUSED [1,2,4]THIADIAZINE DERIVATIVES WHICH ACT AS KAT INHIBITORS OF THE MYST FAMILY
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Page/Page column 103; 104, (2019/03/17)
A compound of formula (I): which inhibits the activity of one or more KATs of the MYST family, i.e., TIP60, KAT6B, MOZ, HBO1 and MOF.
Effect on KATP channel activation properties and tissue selectivity of the nature of the substituent in the 7- and the 3-position of 4H-1,2,4-benzothiadiazine 1,1-dioxides
Boverie, Stéphane,Antoine, Marie-Hélène,Somers, Fabian,Becker, Bénédicte,Sebille, Sophie,Ouedraogo, Raogo,Counerotte, Stéphane,Pirotte, Bernard,Lebrun, Philippe,De Tullio, Pascal
, p. 3492 - 3503 (2007/10/03)
The present work explored 3-alkylamino-4H-1,2,4-benzothiadiazine 1,1-dioxides diversely substituted in the 7-position. Those compounds, structurally related to previously described potassium channel openers such as the benzothiadiazine dioxide BPDZ 73, we
