81549-07-7 Usage
Uses
Used in Pharmaceutical Industry:
ACETOXIME O-(2,4,6-TRIMETHYLPHENYLSULFONATE) is used as a protecting agent for carbonyl groups in the synthesis of pharmaceuticals, allowing for selective reactions and the production of complex molecular structures without interference from reactive functional groups.
Used in Agrochemical Industry:
In the agrochemical industry, ACETOXIME O-(2,4,6-TRIMETHYLPHENYLSULFONATE) is employed as a reagent in the synthesis of agrochemicals, providing protection for carbonyl groups during the production process and enabling the creation of effective and targeted chemical compounds for agricultural applications.
Used in Academic Research:
ACETOXIME O-(2,4,6-TRIMETHYLPHENYLSULFONATE) is utilized in academic research as a tool for studying the reactivity and properties of carbonyl-containing compounds, facilitating the exploration of new chemical reactions and the development of innovative synthetic methods.
Used in Industrial Settings:
In industrial applications, ACETOXIME O-(2,4,6-TRIMETHYLPHENYLSULFONATE) is used as a reagent in the large-scale production of fine chemicals, providing a reliable and efficient means of protecting carbonyl groups during chemical synthesis, thereby enhancing the yield and purity of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 81549-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81549-07:
(7*8)+(6*1)+(5*5)+(4*4)+(3*9)+(2*0)+(1*7)=137
137 % 10 = 7
So 81549-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO3S/c1-8(2)13-16-17(14,15)12-10(4)6-9(3)7-11(12)5/h6-7H,1-5H3
81549-07-7Relevant academic research and scientific papers
Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists
-
, (2008/06/13)
The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.
Synthese et reactivite de quelques α-amino azocomposes: mecanisme de la cyclisation thermique en triazoles-1,2,4
Metra, Pierre,Hamelin, Jack
, p. 285 - 290 (2007/10/02)
The reaction of O-mesitylenesulfonylhydroxylamine (MSH) with hydrazones leads to carbon amination with the formation of α-amino azo compounds.Thermolysis of these compounds affords 1,2,4-triazoles.The mechanism of this cyclization is discussed.
