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4-acetylamino-N-benzooxazol-2-yl-benzenesulfonamide is a complex organic chemical compound with the molecular formula C16H12N2O4S. It is characterized by a benzene ring with a sulfonamide group attached, a benzoxazole ring, and an acetylamino group. 4-acetylamino-N-benzooxazol-2-yl-benzenesulfonamide is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its structure allows for the formation of hydrogen bonds and other interactions, which can be crucial for its biological activity. The compound's properties, such as solubility and stability, can be influenced by the presence of the sulfonamide and acetylamino groups, making it a versatile molecule for further chemical modifications and drug development.

6846-56-6

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6846-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6846-56-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,4 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6846-56:
(6*6)+(5*8)+(4*4)+(3*6)+(2*5)+(1*6)=126
126 % 10 = 6
So 6846-56-6 is a valid CAS Registry Number.

6846-56-6Relevant academic research and scientific papers

The optimization and characterization of functionalized sulfonamides derived from sulfaphenazole against Mycobacterium tuberculosis with reduced CYP 2C9 inhibition

Chen, Hui,Wang, Bin,Li, Peng,Yan, Hong,Li, Gang,Huang, Haihong,Lu, Yu

supporting information, (2021/03/26)

In this study, a series of sulfonamide compounds was designed and synthesized through the systematic optimization of the antibacterial agent sulfaphenazole for the treatment of Mycobacterium tuberculosis (M. tuberculosis). Preliminary results indicate that the 4-aminobenzenesulfonamide moiety plays a key role in maintaining antimycobacterial activity. Compounds 10c, 10d, 10f and 10i through the optimization on phenyl ring at the R2 site on the pyrazole displayed promising antimycobacterial activity paired with low cytotoxicity. In particular, compound 10d displayed good activity (MIC = 5.69 μg/mL) with low inhibition of CYP 2C9 (IC50 > 10 μM), consequently low potential risk of drug-drug interaction. These promising results provide new insight into the combination regimen using sulfonamide as one component for the treatment of M. tuberculosis.

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