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N-(quinoxalin-2-yl)benzenesulfonamide is a chemical compound with the molecular formula C13H10N4O2S. It is a derivative of benzenesulfonamide, featuring a quinoxalin-2-yl group attached to the nitrogen atom. N-(quinoxalin-2-yl)benzenesulfonamide is known for its potential applications in pharmaceutical research, particularly as a building block for the synthesis of various heterocyclic compounds with potential biological activities. The quinoxaline ring system, which is part of the molecule, is a common structural motif in many bioactive molecules, making N-(quinoxalin-2-yl)benzenesulfonamide an interesting target for the development of new drugs and medicinal agents.

6450-63-1

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6450-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6450-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6450-63:
(6*6)+(5*4)+(4*5)+(3*0)+(2*6)+(1*3)=91
91 % 10 = 1
So 6450-63-1 is a valid CAS Registry Number.

6450-63-1Downstream Products

6450-63-1Relevant academic research and scientific papers

Synthesis, antimicrobial activity and quantum calculations of novel sulphonamide derivatives

Fahim, Asmaa M.,Ismael, Eman H.I.

, p. 1427 - 1440 (2019/09/18)

THE nitrogen-based nucleophiles was studied in this investigation and gave the corresponding reactivity of 2-bromo-N-(phenylsulfonyl)acetamide derivatives 3a-c towards some aminothiazole 6a-c, aminooxazole 7a-c, quinazoline-2-yl 10a-c; respectively. Furthermore, the reaction of acetamide derivatives 3a-c with aminopyridine gave pyridine-4-ylamino 12ac. Reaction of acetamide derivatives 3a-c with benzo-2-thiol derivatives afforded benzo [d] thiazol-2-ylthio 14a-c and 1H-benzo[d]imidazol-2-yl)thio derivatives 16a-c; respectively. The synthesized compounds displayed good antimicrobial activity. Additionally, compounds 12a and 14a exhibited high activity towards most of the strains. The computational calculations for 12a and 14a were carried out via HF/6-31G(d) and DFT B3LYP/6-31G(d) basis sets and the corresponding results of HOMO-LUMO energy gap and Mulliken atomic charges were tabulated. This correlation between experimental and theoretical calculations provided a good confirmation for anticipated new compounds.

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