849056-66-2 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Bromo-N-(fur-2-ylmethyl)benzenesulphonamide is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-Bromo-N-(fur-2-ylmethyl)benzenesulphonamide is utilized as a precursor for the production of various agrochemicals. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases in agriculture.
Used as an Antimicrobial Agent:
2-Bromo-N-(fur-2-ylmethyl)benzenesulphonamide is used as an antimicrobial agent due to its ability to inhibit the growth of bacteria and other microorganisms. This property makes it suitable for use in various applications, such as in the development of antimicrobial coatings or in the formulation of disinfectants.
Used as an Antifungal Agent:
The antifungal properties of 2-Bromo-N-(fur-2-ylmethyl)benzenesulphonamide make it a valuable component in the development of antifungal products. It can be used in the treatment of fungal infections or incorporated into materials to prevent fungal growth.
Used in Carbonic Anhydrase Inhibition Research:
2-Bromo-N-(fur-2-ylmethyl)benzenesulphonamide has been studied for its potential use as an inhibitor of carbonic anhydrase, an enzyme that plays a crucial role in various physiological processes. Its ability to inhibit this enzyme could lead to the development of new treatments for conditions related to carbonic anhydrase dysregulation.
Check Digit Verification of cas no
The CAS Registry Mumber 849056-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,5 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 849056-66:
(8*8)+(7*4)+(6*9)+(5*0)+(4*5)+(3*6)+(2*6)+(1*6)=202
202 % 10 = 2
So 849056-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10BrNO3S/c12-10-5-1-2-6-11(10)17(14,15)13-8-9-4-3-7-16-9/h1-7,13H,8H2
849056-66-2Relevant academic research and scientific papers
Diastereoselective synthesis of 1,3-disubstituted isoindolines and sultams via bronsted acid catalysis
Tao, Ye,Gilbertson, Scott R.
supporting information, p. 11292 - 11295 (2018/10/26)
The bis(trifluoromethane)sulfonimide (Tf2NH) catalyzed intramolecular hydroamidation of terminal alkynes is reported. The combination of Et3SiH and Tf2NH provides cis-1,3-disubstituted isoindolines and sultams in high yield (up to 98%) and high diastereoselectivity (up to 99?:?1 d.r.).
