6402-89-7 Usage
Description
Disulfanilamide is a chemical compound that belongs to the class of sulfonamides, known for their antibacterial properties. It is an effective antibiotic used in the treatment of various bacterial infections by inhibiting bacterial growth and proliferation through interference with their metabolic processes.
Uses
Used in Clinical Medicine:
Disulfanilamide is used as an antibiotic for treating a range of bacterial infections, such as urinary tract infections, respiratory infections, and skin infections. It is administered orally and is often combined with other antibiotics to enhance its efficacy in combating bacterial infections.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, disulfanilamide is utilized as a key component in the formulation of various antibacterial drugs. Its combination with other antibiotics allows for a broader spectrum of action and increased effectiveness against resistant bacterial strains.
However, it is important to note that disulfanilamide may cause side effects in some individuals, such as allergic reactions, skin rashes, and gastrointestinal disturbances. Therefore, it is crucial to monitor patients for any adverse reactions during treatment with this antibiotic.
Check Digit Verification of cas no
The CAS Registry Mumber 6402-89-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6402-89:
(6*6)+(5*4)+(4*0)+(3*2)+(2*8)+(1*9)=87
87 % 10 = 7
So 6402-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O4S2/c13-9-1-5-11(6-2-9)20(16,17)15-21(18,19)12-7-3-10(14)4-8-12/h1-8,15H,13-14H2
6402-89-7Relevant articles and documents
Effects of medium and substituents on dissociation of 4,4′-disubstituted bis(benzenesulfon)imides
Ludwig, Miroslav,Stverka, Pavel
, p. 1205 - 1214 (2007/10/03)
Ten 4,4′-disubstituted bis(arenesulfon)imides of the general formula XC6H4SO2NHSO2C6H 4X have been synthesized and their structures confirmed by their 1H NMR spectra. Elemental analyses are presented for the compounds not yet described. The dissociation constants of these model substances have been measured potentiometrically in pyridine, dimethylformamide, methanol, ethanol, propylene carbonate, acetone, acetonitrile, 1,2-dichloroethane and tetramethylene sulfone. The pKHA values obtained have been correlated with three sets of the Hammett substituent constants and the results have been used to discuss the solvent and substituent effects on the dissociation of the compounds studied. Sulfonimides with electron-acceptor substituents behave as rather strong acids in some solvents (pyridine, dimethylformamide, methanol and ethanol), whereas normal substituent dependences are found in other solvents. The experimental data have also been interpreted with the help of the statistical methods based on latent variables. From the calculations it follows that only the first principal component, which correlates well with the substituent constant sets adopted, is statistically significant in describing the substituent effect on the acid-base process studied.