913472-55-6 Usage
Description
3,4,5-Trifluorobenzenesulfonamide is a chemical compound with the molecular formula C6H5F3NO2S. It is a white solid that features a sulfonamide group attached to a benzene ring, with three fluorine atoms positioned at different locations on the ring. 3,4,5-Trifluorobenzenesulfonamide is known for its versatile applications across various industries.
Uses
Used in Pharmaceutical Industry:
3,4,5-Trifluorobenzenesulfonamide is utilized as a building block for the synthesis of pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4,5-Trifluorobenzenesulfonamide serves as a fundamental component in the creation of agrochemicals. Its incorporation aids in the development of effective products for agricultural applications, such as pesticides and herbicides.
Used as an Antimicrobial Agent:
3,4,5-Trifluorobenzenesulfonamide is employed for its antimicrobial properties, making it a valuable asset in combating microbial infections. Its ability to inhibit the growth of microorganisms renders it useful in various sanitizing and preservation processes.
Used as a Reagent in Organic Synthesis:
3,4,5-Trifluorobenzenesulfonamide also functions as a reagent in organic synthesis, facilitating a range of chemical reactions. Its presence can enhance the efficiency and selectivity of these reactions, which is crucial in the production of various organic compounds.
Used as a Catalyst in Chemical Reactions:
3,4,5-Trifluorobenzenesulfonamide is used as a catalyst to accelerate various chemical reactions. Its catalytic properties enable it to lower the energy barrier of reactions, making industrial processes more efficient and sustainable.
Overall, 3,4,5-Trifluorobenzenesulfonamide is a multifaceted chemical with significant applications in the pharmaceutical, agrochemical, and chemical industries, as well as in antimicrobial and synthetic chemistry domains.
Check Digit Verification of cas no
The CAS Registry Mumber 913472-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,4,7 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 913472-55:
(8*9)+(7*1)+(6*3)+(5*4)+(4*7)+(3*2)+(2*5)+(1*5)=166
166 % 10 = 6
So 913472-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F3NO2S/c7-4-1-3(13(10,11)12)2-5(8)6(4)9/h1-2H,(H2,10,11,12)
913472-55-6Relevant articles and documents
Visible Light Mediated Bidirectional Control over Carbonic Anhydrase Activity in Cells and in Vivo Using Azobenzenesulfonamides
, p. 14522 - 14531 (2020)
Two azobenzenesulfonamide molecules with thermally stable cis configurations resulting from fluorination of positions ortho to the azo group are reported that can differentially regulate the activity of carbonic anhydrase in the trans and cis configuratio
