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Benzenesulfonamide, 4-amino-N-[(dimethylamino)methylene]-, also known as Acetazolamide, is a white crystalline powder with the chemical formula C4H7N3O3S2. It is a carbonic anhydrase inhibitor, which means it works by reducing the amount of carbonic anhydrase in the body, an enzyme responsible for producing carbon dioxide. This action helps to decrease the amount of fluid in the body, making it useful in treating conditions such as altitude sickness, glaucoma, and certain types of seizures. Acetazolamide is also used as a diuretic and in the treatment of certain kidney stones. It is available in various forms, including tablets, capsules, and injectable solutions, and is typically taken orally.

6912-49-8

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6912-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6912-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6912-49:
(6*6)+(5*9)+(4*1)+(3*2)+(2*4)+(1*9)=108
108 % 10 = 8
So 6912-49-8 is a valid CAS Registry Number.

6912-49-8Downstream Products

6912-49-8Relevant academic research and scientific papers

Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors

Berrino, Emanuela,Angeli, Andrea,Zhdanov, Dmitry D.,Kiryukhina, Anna P.,Milaneschi, Andrea,De Luca, Alessandro,Bozdag, Murat,Carradori, Simone,Selleri, Silvia,Bartolucci, Gianluca,Peat, Thomas S.,Ferraroni, Marta,Supuran, Claudiu T.,Carta, Fabrizio

, p. 7392 - 7409 (2020/09/12)

Cancer cells rely on the enzyme telomerase (EC 2.7.7.49) to promote cellular immortality. Telomerase inhibitors (i.e., azidothymidine) can represent promising antitumor agents, although showing high toxicity when administered alone. Better outcomes were o

Metal- and solvent-free synthesis of N-sulfonylformamidines

Chandna, Nisha,Chandak, Navneet,Kumar, Pawan,Kapoor, Jitander K.,Sharma, Pawan K.

, p. 2294 - 2301 (2013/09/24)

A solvent-free green synthesis of N-sulfonylformamidines is reported via the direct condensation of N,N-dimethylformamide dimethyl acetal (DMF-DMA) and sulfonamide derivatives at room temperature. The described method avoids the use of metal catalysts as

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