217813-03-1 Usage
Uses
Used in Chemical Synthesis:
3-Methoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate, 95.0+%(GC) is used as a reagent in chemical synthesis processes for its reactivity and high purity. The trifluoromethanesulfonate group allows for efficient reactions with various substrates, making it a valuable component in the synthesis of complex organic molecules.
Used in Laboratory Research:
In laboratory settings, 3-Methoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate, 95.0+%(GC) is used as a research chemical to study its properties and potential applications. The high purity of the compound ensures accurate results in experiments, and its reactivity allows for exploration of its behavior in different chemical environments.
Used in Industrial Applications:
3-Methoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate, 95.0+%(GC) is employed in industrial applications where its reactivity and high purity are advantageous. 3-METHOXY-2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE,95.0+%(GC) may be used in the production of pharmaceuticals, agrochemicals, or other specialty chemicals, where its unique properties contribute to the efficiency and effectiveness of the manufacturing process.
Check Digit Verification of cas no
The CAS Registry Mumber 217813-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,8,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 217813-03:
(8*2)+(7*1)+(6*7)+(5*8)+(4*1)+(3*3)+(2*0)+(1*3)=121
121 % 10 = 1
So 217813-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H15F3O4SSi/c1-17-8-6-5-7-9(10(8)20(2,3)4)18-19(15,16)11(12,13)14/h5-7H,1-4H3
217813-03-1Relevant articles and documents
Total Syntheses of Aporphine Alkaloids via Benzyne Chemistry: An Approach to the Formation of Aporphine Cores
Rossini, Allan F. C.,Muraca, Ana Carolina A.,Casagrande, Gleison A.,Raminelli, Cristiano
, p. 10033 - 10040 (2015)
Total syntheses of lysicamine, (±)-nuciferine, (±)-nornuciferine, (±)-zanthoxyphylline iodide, (±)-O-methylisothebaine, and (±)-trimethoxynoraporphine were accomplished by an approach that involves the formation of aporphine cores through reactions betwee
Synthesis of o-Aryloxy Triarylsulfonium Salts via Aryne Insertion into Diaryl Sulfoxides
Li, Xiaojin,Sun, Yan,Huang, Xin,Zhang, Lei,Kong, Lichun,Peng, Bo
, p. 838 - 841 (2017/02/26)
The aryne insertion into "S-O" bond has been validated recently. This technology is elusively applied to the synthesis of thioethers. In contrast to the reported cases, the reaction described furnished o-aryloxy triarylsulfonium salts, in lieu of thioethe
