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151072-61-6

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151072-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151072-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,7 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 151072-61:
(8*1)+(7*5)+(6*1)+(5*0)+(4*7)+(3*2)+(2*6)+(1*1)=96
96 % 10 = 6
So 151072-61-6 is a valid CAS Registry Number.

151072-61-6Relevant articles and documents

Synthesis of the laminara-oligosaccharide methyl β-glycosides of dp 3-8

Takeo,Maki,Wada,Kitamura

, p. 81 - 96 (2007/10/02)

Ethyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-glucopyranoside has been prepared in a good yield by anomerization of the corresponding β-thioglucoside with tin(IV) chloride and transformed, in three steps, into ethyl 2-O-benzoyl-4,6-O-benzylidene-1-thio-α-D-glucopyranoside (18). Chloroacetylation of 18, followed by treatment of the product with chlorine gave crystalline 2-O-benzoyl-4,6-O-benzylidene-3-O-chloroacetyl-β-D-glucopyranosyl chloride (20). This was coupled with methanol in the presence of silver carbonate-silver perchlorate and the product was O-dechloroacetylated to afford methyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside (22). Silver triflate-promoted glucosylation of 18 with 20 gave a β-(1 → 3)-linked disaccharide derivative, reaction of which with chlorine yielded crystalline O-(2-O-benzoyl-4,6-O-benzylidene-3-O-chloroacetyl-β-D-glucopyranosyl) -(1 → 3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl chloride (24). Likewise, condensation of 22 with 20 gave a β-(1 → 3)linked disaccharide glycoside, which was partially deprotected to give methyl O-(2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1 → 3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside (26). The methyl β-glycosides of a homologous series of (1 → 3)-linked β-D-gluco-oligosaccharides from the tri- to the octa-saccharide have been synthesized in a blockwise manner by using 22 and 26 as the glycosyl acceptors, 24 as the disaccharide donor, and silver triflate as the promoter. Ethyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-glucopyrano- side has been prepared in a good yield by anomerization of the corresponding B-thioglucoside with tin(IV) chloride and transformed, in three steps.

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