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dimethyl(thexyl)silyl 3-O-acetyl-6-O-benzoyl-2-deoxy-2-dimethylmaleimido-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

315208-40-3

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315208-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315208-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,2,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 315208-40:
(8*3)+(7*1)+(6*5)+(5*2)+(4*0)+(3*8)+(2*4)+(1*0)=103
103 % 10 = 3
So 315208-40-3 is a valid CAS Registry Number.

315208-40-3Relevant academic research and scientific papers

Synthesis of an asparagine-linked heptasaccharide - Basic structure of N-glycans

Chiesa, M. Vittoria,Schmidt, Richard R.

, p. 3541 - 3554 (2007/10/03)

Galβ(1-4)GlcNAcβ(1-2)Manα(1-3)[Manα(1-6)]Manβ(1-4)-GlcNAcβ(1-4)GlcNAcβ (1-N)Asn (1) was disconnected into building blocks 2-6. N-Dimethylmaleoyl (DMM) protected glucosamine 3 was readily obtained from glucosamine. Transformation of 3 into 4-O-unprotected glucosamine derivatives 9, 14, and 18 furnished the intermediates required for the incorporation of the three differently linked glucosamine residues. Thus, disaccharide 20 was obtained from acceptor 9 and glucosyl donor 19 and converted into protected Manβ(1-4)GlcNAc disaccharide donor 5 by inversion of the configuration at C-2 of the glucose residue. Glycosylation of acceptor 18 with known galactosyl donor 26 afforded protected lactosamine donor 6. The synthesis of asparagine building block 2 and of mannosyl donor 4 has already been reported. With building blocks 2-6 in hand, the synthesis of 1 was accomplished. Glycosylation of acceptor 14 with donor 5 gave trisaccharide 29 which was transformed into acceptor 30. Treatment of 30 with glycosyl donor 4 provided tetrasaccharide intermediate 31. Its transformation into 2d-O-unprotected acceptor 33 and then reaction with disaccharide donor 6 furnished hexasaccharide 34. Removal of the 4c,6c-O-benzylidene group gave 4c,6c-O-unprotected acceptor 35 which, on glycosylation with donor 4, led to heptasaccharide 36. Replacement of the N-DMM groups by N-acetyl groups and removal of all O-acyl groups, followed by transformation of the C-1a azido group into an amino group, and attachment of asparagine building block 2 led to the desired heptasaccharide β-linked to asparagine 39. Hydrogenolysis of all O-benzyl groups afforded target molecule 1.

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