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2-((Benzyloxy)methyl)-1-((α-(trimethylsilyl)benzyl)sulfonyl)pyrrolidine is a complex organic compound with the molecular formula C23H31NOSS2i. It features a pyrrolidine ring, which is a five-membered nitrogen-containing ring, with a benzyloxymethyl group attached to the 2-position. The 1-position is substituted with a sulfonyl group, which is connected to an α-(trimethylsilyl)benzyl moiety. 2-((Benzyloxy)methyl)-1-((α-(trimethylsilyl)benzyl)sulfonyl)pyrrolidine is characterized by its unique structure, which includes a sulfonyl bridge and a trimethylsilyl group, providing it with potential applications in organic synthesis and as a precursor in the preparation of various pharmaceuticals and chemical intermediates. Its synthesis and reactivity can be influenced by the electronic and steric properties of the substituents, making it a subject of interest in the field of organic chemistry.

89598-20-9

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89598-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89598-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,9 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89598-20:
(7*8)+(6*9)+(5*5)+(4*9)+(3*8)+(2*2)+(1*0)=199
199 % 10 = 9
So 89598-20-9 is a valid CAS Registry Number.

89598-20-9Relevant academic research and scientific papers

Asymmetric Diels-Alder Reactions with Sulfines Derived from Proline

Broek, Leon A. G. M. van den,Porskamp, Pascal A. T. W.,Haltiwanger, R. Curtis,Zwanenburg, Binne

, p. 1691 - 1695 (2007/10/02)

The Synthesis of a variety of sulfines 8 derived from S-proline, utilizing the reaction of α-silyl carbanions with sulfur dioxide, is described.Reaction of the thus prepared sulfines 8 with 2,3-dimethyl-1,3-butadiene gave dihydrothiopyran S-oxides 9.During these cycloaddition reactions asymmetric inductions up to 40percent were observed.From one pure diastereomeric form of cycloadduct 9d an X-ray analysis was carried out in order to provide insight in the steric course of the cycloaddition reaction.

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