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Methyl β-D-glucopyranosyl-(1->4)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranoside is a complex carbohydrate molecule, specifically a type of polysaccharide. It consists of four β-D-glucopyranosyl units linked together in a linear fashion through (1->4) glycosidic bonds, with a methyl group attached to the anomeric carbon of the terminal glucose unit. This structure is a derivative of maltotetraose, a natural disaccharide found in the hydrolysis of starch, with an additional two glucose units and a methyl group. The compound is of interest in the field of organic chemistry, particularly in the study of carbohydrates and their derivatives, and may have potential applications in pharmaceuticals, food science, and materials science due to its unique structure and properties.

5602-00-6

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5602-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5602-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5602-00:
(6*5)+(5*6)+(4*0)+(3*2)+(2*0)+(1*0)=66
66 % 10 = 6
So 5602-00-6 is a valid CAS Registry Number.

5602-00-6Downstream Products

5602-00-6Relevant academic research and scientific papers

Optimized synthesis of specific sizes of maltodextrin glycosides by the coupling reactions of Bacillus macerans cyclomaltodextrin glucanyltransferase

Yoon, Seung-Heon,Robyt, John F.

, p. 210 - 217 (2006)

Bacillus macerans cyclomaltodextrin glucanyltransferase (CGTase, EC 2.4.1.19), in reaction with cyclomaltohexaose and methyl α-d- glucopyranoside, methyl β-d-glucopyranoside, phenyl α-d- glucopyranoside, and phenyl β-d-glucopyranoside gave four kinds of maltodextrin glycosides. The reactions were optimized by using different ratios of the individual d-glucopyranosides to cyclomaltohexaose, from 0.5 to 5.0, to obtain the maximum molar percent yields of products, which were from 68.3% to 78.6%, depending on the particular d-glucopyranoside, and also to obtain different maltodextrin chain lengths. The lower ratios of 0.5-1.0 gave a wide range of sizes from d.p. 2-17 and higher. As the molar ratio was increased from 1.0 to 3.0, the larger sizes, d.p. 9-17, decreased, and the small and intermediate sizes, d.p. 2-8, increased; as the molar ratios were increased further from 3.0 to 5.0, the large sizes completely disappeared, the intermediate sizes, d.p. 4-8, decreased, and the small sizes, d.p. 2 and 3 became predominant. A comparison is made with the synthesis of maltodextrins by the reaction of CGTase with different molar ratios of d-glucose to cyclomaltohexaose.

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