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3,5-di-O-benzyl-6-O-(tert-butyldiphenylsilyl)-1,2-O-isopropylidene-α-D-allofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

217089-45-7

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217089-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217089-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,0,8 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 217089-45:
(8*2)+(7*1)+(6*7)+(5*0)+(4*8)+(3*9)+(2*4)+(1*5)=137
137 % 10 = 7
So 217089-45-7 is a valid CAS Registry Number.

217089-45-7Relevant academic research and scientific papers

Synthesis of 6,6'-ether linked disaccharides from D-allose, D-galactose, D-glucose and D-mannose; evidence on the structure of coyolosa.

Haines, Alan H

, p. 2352 - 2358 (2007/10/03)

6,6'-Linked ethers derived from D-allose, D-galactose, D-glucose, and D-mannose have been prepared in order to allow comparisons with the reported 6,6'-linked hexopyranose coyolosa, an hypoglycemic compound which has been isolated by extraction of the roo

Evidence on the structure of coyolosa. Synthesis of 6,6′-ether linked hexoses

Haines, Alan H.

, p. 835 - 837 (2007/10/03)

The structure previously reported for coyolosa, a hypoglycemic substance isolated from natural sources, as a 6,6′-ether linked pseudo-disaccharide derived from allose, is incorrect since 6-O-(6-deoxy-D-allos-6-yl)-D-allose 10, synthesised by an unequivoca

Synthesis of tetrahydropyrans from sugar lactones

Estevez, Juan C.,Fairbanks, Antony J.,Fleet, George W.J.

, p. 13591 - 13620 (2007/10/03)

Dehydration of both γ- and δ- hexonolactones, either by intramolecular nucleophilic displacement of triflate leaving groups at C-2, or by Mitsunobu type displacement of the OH-6, provides access to bicyclic lactones which contain tetrahydropyran rings. Reduction or nucleophilic ring opening of these bicyclic lactones furnishes polyfunctionalised tetrahydropyrans in good yield.

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