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methyl (4-O-benzoyl-3-O-benzyl-2-O-acetyl-α-L-rhamnopyranosyl)-(1->4)-2,3-di-O-benzyl-α-D-galactopyranuronate trichloroacetimidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

406460-75-1

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406460-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406460-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,4,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 406460-75:
(8*4)+(7*0)+(6*6)+(5*4)+(4*6)+(3*0)+(2*7)+(1*5)=131
131 % 10 = 1
So 406460-75-1 is a valid CAS Registry Number.

406460-75-1Downstream Products

406460-75-1Relevant academic research and scientific papers

Block synthesis with galacturonate trichloroacetimidates

Nolting, Birte,Boye, Hanna,Vogel, Christian

, p. 585 - 610 (2007/10/03)

The disaccharide methyl (4-O-benzoyl-3-O-benzyl-2-O-acetyl-α-L-rhamno pyranosyl)-(1→4)-(allyl 2,3-di-O-benzy-β-D-galactopyranosid)uronate (13) was obtained in an excellent yield of 88% using methyl (allyl 2,3-di-O-benzyl-β-D-galactopyranosid)uronate (12) as the glycosyl acceptor and a slight excess of the 1,2-di-O-acetyl-rhamnoglycosyl donor 5a. Disaccharide 13 is a key intermediate that can be used either as a glycosyl acceptor or glycosyl donor for the preparation of rhamnogalacturonan fragments. Here, introduction of the trichloroacetimidate function at the anomeric center gave the disaccharide glycosyl donor 28, which could be applied in a blockwise glycosylation reaction to form the L-Rha-α(1→4)-D-GalA-α(1→4)-D-GalA trisaccharide 29. Generally, on condition that no neighboring group effect influenced the reaction at the anomeric center of the α-trichloroacetimidate galacturonate glycosyl donors (20-22,28), α-glycosidic linkages were nearly exclusively formed, except in the case of the 4-O-methylgalactopyranosyluronate 22.

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