6341-35-1 Usage
Uses
Used in Pharmaceutical Industry:
4-Fluoro-N-(furan-2-ylmethyl)benzenesulfonamide is used as a chemical intermediate for the synthesis of pharmaceuticals, particularly for the development of antimicrobial agents. Its sulfonamide structure contributes to its potential as an active ingredient in medications targeting bacterial infections.
Used in Chemical Research:
4-Fluoro-N-(furan-2-ylmethyl)benzenesulfonamide is used as a research compound in the field of organic chemistry, where its unique structure and properties are studied for potential applications in the synthesis of new molecules and materials.
Used in Material Science:
4-Fluoro-N-(furan-2-ylmethyl)benzenesulfonamide is used as a building block in the development of new materials, such as polymers and composites, that can benefit from its electron-rich and heteroaromatic characteristics. This can lead to advancements in areas like electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 6341-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6341-35:
(6*6)+(5*3)+(4*4)+(3*1)+(2*3)+(1*5)=81
81 % 10 = 1
So 6341-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H10FNO3S/c12-9-3-5-11(6-4-9)17(14,15)13-8-10-2-1-7-16-10/h1-7,13H,8H2
6341-35-1Relevant academic research and scientific papers
Banning, Joseph E.,Gentillon, Jacob,Ryabchuk, Pavel G.,Prosser, Anthony R.,Rogers, Andrew,Edwards, Andrew,Holtzen, Andrew,Babkov, Ivan A.,Rubina, Marina,Rubin, Michael
, p. 7601 - 7616 (2013)
A highly chemo- and diastereoselective protocol toward amino-substituted donor-acceptor cyclopropanes via the formal nucleophilic displacement in bromocyclopropanes is described. A wide range of N-nucleophiles, including carboxamides, sulfonamides, azoles, and anilines, can be efficiently employed in this transformation, providing expeditious access to stereochemically defined and densely functionalized cyclopropylamine derivatives.
