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phenoxy-acetic acid 7-{2,3-dimethoxy-2,3,5-trimethyl-7-[4-(2-octadecyloxy-1-octadecyloxymethyl-ethoxymethyl)-benzyloxy]-hexahydro-pyrano[3,4-b][1,4]dioxin-8-yloxy}-2,3-dimethoxy-2,3,5-trimethyl-hexahydro-pyrano[3,4-b][1,4]dioxin-8-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

854936-89-3

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854936-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854936-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,9,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 854936-89:
(8*8)+(7*5)+(6*4)+(5*9)+(4*3)+(3*6)+(2*8)+(1*9)=223
223 % 10 = 3
So 854936-89-3 is a valid CAS Registry Number.

854936-89-3Relevant academic research and scientific papers

Hydrophobically assisted switching phase synthesis: The flexible combination of solid-phase and solution-phase reactions employed for oligosaccharide preparation

Bauer, Joerg,Rademann, Joerg

, p. 7296 - 7297 (2007/10/03)

Hydrophobically assisted switching phase (HASP) synthesis is a concept that allows the choice between the advantages of solid-supported chemistry and those of solution-phase synthesis. Starting from the examination of adsorption and desorption properties of hydrophobic molecules to and from reversed-phase silica, we designed a dilipid as a quantitative and fully reversible HASP anchor, permitting final product release. The utility of this new tool in synthetic organic chemistry was demonstrated on oligosaccharide preparation. The synthesis of a pentarhamnoside was accomplished by repetitive glycosylation reactions. Glycosylations were conducted preferably in solution, whereas all protecting group manipulations were performed on solid support. Without the need for chromatographic purification of intermediates, the HASP system furnished the final product after 12 linear steps with average yields of 94% per step at a scale of 0.1 mmol, thus overcoming several of the limitations encountered in the solid-phase synthesis of complex carbohydrates. Copyright

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