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methyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-methyl-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1335014-67-9

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1335014-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1335014-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,0,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1335014-67:
(9*1)+(8*3)+(7*3)+(6*5)+(5*0)+(4*1)+(3*4)+(2*6)+(1*7)=119
119 % 10 = 9
So 1335014-67-9 is a valid CAS Registry Number.

1335014-67-9Downstream Products

1335014-67-9Relevant academic research and scientific papers

Synthesis of blockwise alkylated (1→4) linked trisaccharides as surfactants: Influence of configuration of anomeric position on their surface activities

Nakagawa, Atsushi,Kamitakahara, Hiroshi

experimental part, p. 1671 - 1683 (2011/11/12)

New carbohydrate-based surfactants consisting of hydrophilic cellobiosyl and hydrophobic glucosyl residues, methyl β-D-glucopyranosyl-(1→4)- α-D-glucopyranosyl-(1→4)-2,3,6-tri-O-methyl-α-D- glucopyranoside 1 (GβGαMα, G: glucopyranosyl residue, α and β: α-(1→4)- and β-(1→4) glycosidic bonds, M: methyl group), 2 (GβGβMα), 3 (GβGαMβ), 4 (G βGβMβ), 5 (G βGαEα, E: ethyl group), 6 (GβGβEα), 7 (G βGαEβ), 8 (G βGβEβ) and eight α-and β-glycoside mixtures (a mixture of 1 and 2: 1/2 = 62/38 (9), 32/68 (10); a mixture of 3 and 4: 3/4 = 69/31 (11), 32/68 (12); a mixture of 5 and 6: 5/6 = 62/38 (13), 33/67 (14); a mixture of 7 and 8: 7/8 = 59/41 (15), 29/71 (16)) were synthesized via combined methods consisting of acid-catalyzed alcoholysis of cellulose ethers and glycosylation of phenyl thio-cellobioside derivatives. Their surface activities in aqueous solution depended on their chemical structures: α- or β-(1→4) linkage between hydrophilic cellobiosyl and hydrophobic glucosyl blocks, methyl or ethyl groups of hydrophobic glucosyl block, and α- or β-linked ether group at the C-1 of hydrophobic glucosyl block. The mixing effect of α- and β-glycosides on surface activities was also investigated. As a result, ethyl β-D-glucopyranosyl-(1→4)-α-Dglucopyranosyl-(1→4)-2,3, 6-tri-O-ethyl-β-D-glucopyranoside 7 (GβG αEβ) had the highest surface activity, and its critical micellar concentration (CMC) and γCMC (surface tension at CMC) values of compound 7 were 0.5 mM(ca. 0.03 wt %) and 34.5 mN/m, respectively. The surface tensions of α- and β-glycoside mixtures except for compounds 9 and 10 were almost equal to those of pure compounds. The syntheses of the mixtures of α- and β-glycosides without purification process are easier than those of pure compounds. Thus, the mixtures should be more practical compounds for industrial use as a surfactant.

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