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6'-O-tert-butyldiphenylsilyl-2,3,4,6,1',3',4'-hepta-O-benzoylsucrose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81086-94-4

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81086-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81086-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,8 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81086-94:
(7*8)+(6*1)+(5*0)+(4*8)+(3*6)+(2*9)+(1*4)=134
134 % 10 = 4
So 81086-94-4 is a valid CAS Registry Number.

81086-94-4Downstream Products

81086-94-4Relevant academic research and scientific papers

Porphyrins with directly meso -attached disaccharide moieties: Synthesis, self-assembly and cellular study

Malachowska, Magdalena,Sperduto, Claudio,Darmostuk, Mariia,Monti, Donato,Venanzi, Mariano,Mancini, Giovana,D'Acunto, Cosimo Walter,Králová, Jarmila,Ruml, Tomá?,Wimmer, Zdeněk,Dra?ar, Pavel B.

, p. 773 - 784 (2016/11/04)

A series of porphyrins with directly meso-attached "sucrose" moiety by the carbon C-6′ of its "fructose" end was synthesized, and their physico-chemical and aggregation properties studied by spectroscopic (fluorescence, circular dichroism, resonance light scattering) techniques. The effect of selected porphyrins on tumor cells was also evaluated.

Synthesis of 6′-deoxy-6′-fluorosucrose

Gaddam, Vikram,Harmata, Michael

, p. 38 - 41 (2013/05/09)

A facile synthesis of 6′-deoxy-6′-fluorosucrose has been developed. The title compound is available in six linear steps in 44% overall yield from commercially available sucrose. The synthesis involves rapid and convenient fluorination and deprotection con

SYNTHESIS AND REACTIONS OF tert-BUTYLDIPHENYLSILYL ETHERS OF SUCROSE

Karl, Horst,Lee, Cheang Kuan,Khan, Riaz

, p. 31 - 38 (2007/10/02)

The reaction of sucrose with 1.1 mol. equiv. of tert-butyldiphenylsilyl (t-BDPS) chloride in pyridine in the presence of 4-dimethylaminopyridine gave the crystalline 6'-t-BDPS ether 1 in 49percent yield, without recourse to column chromatography.Compound 1 was transformed into the 4,6,1'-trichloride by using sulphuryl chloride.When the silylation reaction of sucrose was performed with 3 mol. equiv. of the reagent, chromatography gave the crystalline 6,6'-di-t-BDPS ether and the 6,1',6'-tri-t-BDPS ether 9 in yield of 78 and 18.7percent, respectively.Compound 9 was obtained as the major product on treatment of sucrose with 4.6 mol.equiv. of the silylating reagent.Removal of the silyl protecting-group in 6,6'-di-O-ter-butyldiphenylsilylsucrose hexabenzoate, using tetrabutylammonium fluoride, proceeded smoothly, but with 4->6 migration of the benzoate.

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