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α-Glucosyl glycerol is a naturally occurring glycolipid found in various plants, particularly in the leaves of the mulberry tree. It is formed by the glycosylation of glycerol with a glucose molecule, resulting in a unique structure that exhibits potential bioactivity. α-glucosyl glycerol has garnered interest due to its potential applications in the pharmaceutical and cosmetic industries, as it is believed to possess anti-inflammatory, antioxidant, and skin-whitening properties. α-Glucosyl glycerol is also being studied for its role in plant defense mechanisms against environmental stressors. Its chemical structure, which includes a glycerol backbone with a glucose molecule attached at the α-position, contributes to its unique properties and potential benefits.

2949-61-3

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2949-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2949-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2949-61:
(6*2)+(5*9)+(4*4)+(3*9)+(2*6)+(1*1)=113
113 % 10 = 3
So 2949-61-3 is a valid CAS Registry Number.

2949-61-3Upstream product

2949-61-3Downstream Products

2949-61-3Relevant academic research and scientific papers

INTERACTION OF (1->4)- AND (1->6)-LINKED DISSACHARIDES WITH THE FENTON REAGENT UNDER PHYSIOLOGICAL CONDITIONS

Uchida, Koji,Kawakishi, Shunro

, p. 89 - 100 (2007/10/02)

Reactions of (1->4) and (1->6)-linked disaccharides, mainly of maltose and isomaltose, with the Fenton reagent under physiologigal conditions were studied.Chemical characterization of oxidation products was conducted by g.l.c. and g.l.c.-m.s. of their trimethylsilyl derivatives, and the results demonstrated that (1->6)-linked disaccharides are more reactive with the hydroxyl radical (.OH) generated by the Fenton reagent than (1->4)-linked disaccharides.About 35-40percent of (1->6)- and 15-20percent of (1->4)-linked disaccharides were oxydatively degraded to smaller molecules after incubation for 24 h.Of the four disaccharides examined, namely, maltose, isomaltose, cellobiose, and gentiobiose, the α-(1->6)-linked disaccharide isomaltose exhibited the highest reactivity, whereas the β-(1->4)-linked disaccharide cellobiose showed the lowest.These results suggest the exisence of the a relationship between the configuration of the glycosidic linkage and the reactivity with .OH in aqueous solution.

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