951883-93-5 Usage
Uses
Used in Pharmaceutical Industry:
N-Cyclopropyl 2-bromobenzenesulfonamide is used as a potential drug candidate for its antimicrobial properties, given its classification within the sulfonamide class of compounds. Its unique structural features, including the cyclopropyl group and bromine atom, may contribute to its effectiveness in treating microbial infections.
Used in Organic Synthesis:
In the field of organic synthesis, N-Cyclopropyl 2-bromobenzenesulfonamide is utilized as an intermediate. Its specific chemical properties and reactivity make it a valuable component in the synthesis of more complex organic compounds, potentially leading to the development of new pharmaceuticals or other chemical products.
Used in Medicinal Chemistry Research:
N-Cyclopropyl 2-bromobenzenesulfonamide is employed in medicinal chemistry research to explore its potential as a new therapeutic agent. Further studies are required to understand its mechanism of action, efficacy, and safety profile, which will determine its suitability for clinical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 951883-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,8,8 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 951883-93:
(8*9)+(7*5)+(6*1)+(5*8)+(4*8)+(3*3)+(2*9)+(1*3)=215
215 % 10 = 5
So 951883-93-5 is a valid CAS Registry Number.
951883-93-5Relevant articles and documents
Diastereoselective Photoredox-Catalyzed [3 + 2] Cycloadditions of N-Sulfonyl Cyclopropylamines with Electron-Deficient Olefins
White, Dawn H.,Noble, Adam,Booker-Milburn, Kevin I.,Aggarwal, Varinder K.
supporting information, p. 3038 - 3042 (2021/05/04)
A highly diastereoselective, visible-light-induced [3 + 2] cycloaddition between N-sulfonyl cyclopropylamines and electron-deficient olefins is reported. The reactions proceed via the oxidation of a sulfonamide aza-anion by an organic photocatalyst to generate a nitrogen-centered radical. Strain-induced ring opening and intermolecular addition to the olefin generate an intermediate carbon-centered radical that is reduced to an anion prior to 5-exo cyclization. This enables a highly diastereoselective construction of trans-cyclopentanes possessing synthetically useful functional groups.
FLAP MODULATORS
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Paragraph 0197; 0199, (2015/11/03)
The present invention relates to compounds of Formula (I), or a form thereof, wherein ring A, R1, R2, R3, R3′, L, W, and V are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention