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The chemical compound "(2S,3R,4S,5R)-4-[(2R,3R,4S,5R,6R)-3,4-Dihydroxy-6-hydroxymethyl-5-((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexane-1,2,3,5,6-pentaol" is a complex, chiral molecule with a unique structure. It consists of a hexane backbone with five hydroxyl groups and two tetrahydro-pyran rings, each containing multiple hydroxyl and hydroxymethyl substituents. The stereochemistry is specified by the R and S configurations at various carbon centers, indicating the three-dimensional arrangement of the atoms. (2S,3R,4S,5R)-4-[(2R,3R,4S,5R,6R)-3,4-Dihydroxy-6-hydroxymethyl-5-((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-hexane-1,2,3,5,6-pentaol is likely to be found in nature, as its intricate structure suggests a role in biological systems, possibly as a component of a larger molecule or a metabolite.

6918-42-9

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6918-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6918-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6918-42:
(6*6)+(5*9)+(4*1)+(3*8)+(2*4)+(1*2)=119
119 % 10 = 9
So 6918-42-9 is a valid CAS Registry Number.

6918-42-9Upstream product

6918-42-9Downstream Products

6918-42-9Relevant academic research and scientific papers

4-O-α-D-GALACTOPYRANOSYL-D-GALACTOSE: EFFICIENT SYNTHETIC ROUTES FROM "POLYGALACTURONIC ACID"

Dahmen, Jan,Frejd, Torbjoern,Lave, Thomas,Lindh, Frank,Magnusson, Goeran,et al.

, p. 219 - 224 (2007/10/02)

Enzymic hydrolysis of "polygalacturonic acid" gave a mixture of oligomers which was fractionated by ion-exchange chromatography.The resulting di- and trisaccharides were treated, respectively, with methanol and ethylene oxide, and the resulting esters were reduced with sodium borohydride.Treatment of the products with acetic anhydride and sulfuric acid, followed by deacetylation, produced the title compound.

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