71270-62-7 Usage
Usage in synthesis
Pharmaceutical and organic intermediate 2-[(methylsulfonyl)amino]phenyl methanesulfonate is used as a building block in the synthesis of pharmaceuticals and serves as an intermediate in organic synthesis processes.
Herbicidal properties
Sulfonylurea herbicide 2-[(methylsulfonyl)amino]phenyl methanesulfonate is a type of sulfonylurea herbicide, which means it is used in agriculture to control and manage certain types of weeds.
Environmental concerns
Potential toxic effects on aquatic organisms 2-[(methylsulfonyl)amino]phenyl methanesulfonate can have harmful effects on aquatic life, so it should be handled with care to minimize its impact on the environment.
Antimicrobial properties
Potential use in antibacterial or antifungal drugs 2-[(methylsulfonyl)amino]phenyl methanesulfonate has been found to exhibit antimicrobial properties, making it a potentially valuable substance in the development of new drugs to combat bacterial and fungal infections.
Check Digit Verification of cas no
The CAS Registry Mumber 71270-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,7 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71270-62:
(7*7)+(6*1)+(5*2)+(4*7)+(3*0)+(2*6)+(1*2)=107
107 % 10 = 7
So 71270-62-7 is a valid CAS Registry Number.
71270-62-7Relevant academic research and scientific papers
Rearrangement of differentially protected N-arylhydroxylamines
Porzelle, Achim,Woodrow, Michael D.,Tomkinson, Nicholas C. O.
experimental part, p. 5135 - 5143 (2009/06/17)
The rearrangement of a series of N,O-difunctionalised N-arylhydroxylamines to generate protected 2-aminophenols has been investigated. N-Boc-N-Aryl-O- acylhydroxylamines are stable, isolable compounds which rearrange smoothly at temperatures between 110 and 140°C. The corresponding N-Boc-N-aryl-O- sulfonylhydroxylamines were not isolated and rearrange to 1,2-difunctionalised aminophenols at room temperature in excellent yield. Deprotection of either the N- or O-substituents under standard conditions allows for further synthetic manipulation of either the aniline or phenol functionality. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
