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2-Methansulfonylamino-benzoesaeurehydrazid, also known as 2-(methylsulfonylamino)benzoic acid hydrazide, is a chemical compound with the molecular formula C8H10N2O3S. It is a white crystalline solid that is soluble in water and various organic solvents. 2-Methansulfonylamino-benzoesaeurehydrazid is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure features a benzoic acid core with a methylsulfonylamino group attached to the 2-position and a hydrazide group at the carboxyl end. The compound's reactivity and versatility make it a valuable building block in organic synthesis, particularly in the preparation of various heterocyclic compounds and drug candidates.

716-40-5

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716-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 716-40-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 716-40:
(5*7)+(4*1)+(3*6)+(2*4)+(1*0)=65
65 % 10 = 5
So 716-40-5 is a valid CAS Registry Number.

716-40-5Downstream Products

716-40-5Relevant academic research and scientific papers

Exploiting oxadiazole-sulfonamide hybrids as new structural leads to combat diabetic complications via aldose reductase inhibition

Chaudhry, Faryal,Imran, Aqeel,Iqbal, Jamshed,Javid, Noman,Munir, Rubina,Muzaffar, Ayesha,Zaib, Sumera

, (2020)

A series of oxadiazole-sulfonamide hybrids was synthesized through multistep reaction and for the formation of targeted thioethers 6(a-l), a much facile route was adopted through which S-alkylation was successfully carried out at room temperature. These novel thioethers 6(a-l) were later screened against aldehyde reductase (ALR1) and aldose reductase (ALR2). Beside the enzyme inhibition studies, the compounds were also tested against cervical cancer cell lines (HeLa). The results suggested the significant inhibition pattern towards ALR2, while few compounds were active against ALR1. The synthesized derivatives have shown weak to moderate cytotoxicity. The most potent inhibitors (6b, 6e, 6f and 6l) were selected for molecular docking studies and the binding interactions were reported.

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