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The chemical compound in question is a complex organic molecule, specifically a derivative of cyclohexane with a hexa-D-glucopyranosyl structure. It is denoted as [1,2,3,4,5,6]O6-hexakis-(toluene-4-sulfonyl)-cyclo-lin-hexa[1α=>4]-D-glucopyranosyl. [1,2,3,4,5,6]O6-hexakis-(toluene-4-sulfonyl)-cyclo-lin-hexa[1α=>4]-D-glucopyranosyl features a cyclohexane ring with six oxygen atoms (O6) and six toluene-4-sulfonyl groups attached to the oxygen atoms. The term "hexakis" indicates that there are six of these toluene-4-sulfonyl groups. The "cyclo-lin-hexa[1α=>4]-D-glucopyranosyl" part of the name suggests a linear arrangement of six D-glucopyranosyl units in a cyclic manner, with the 1α position being connected to the 4 position, forming a specific type of glycosidic linkage. [1,2,3,4,5,6]O6-hexakis-(toluene-4-sulfonyl)-cyclo-lin-hexa[1α=>4]-D-glucopyranosyl is likely to be used in advanced chemical research or as a building block for more complex molecules, given its intricate structure and the presence of multiple functional groups.

21884-25-3

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21884-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21884-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,8 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21884-25:
(7*2)+(6*1)+(5*8)+(4*8)+(3*4)+(2*2)+(1*5)=113
113 % 10 = 3
So 21884-25-3 is a valid CAS Registry Number.

21884-25-3Downstream Products

21884-25-3Relevant academic research and scientific papers

Molecular recognition by self-assembled monolayers of cyclodextrin on Ag

Yamamoto,Maeda,Kitano

, p. 6855 - 6860 (1997)

Self-assembled monolayer (SAM) of a thiolated cyclodextrin (CD) derivative was prepared, and stereoselective inclusional complexation of optically active azo dyes (p- or o-methyl red conjugates with chiral 1-phenyl-ethylamine, p- or o-MR-PEA) with both fr

Polycationic glycosides

Engel, Robert,Ghan, Ishrat,Montenegro, Diego,Thomas, Marie,Klaritch-Vrana, Barbara,Castano, Alejandra,Friedman, Laura,Leb, Jay,Rothman, Leah,Lee, Heidi,Capodiferro, Craig,Ambinder, Daniel,Cere, Eva,Awad, Christopher,Sheikh, Faiza,Rizzo Lee, Jaime,Nisbett, Lisa-Marie,Testani, Erika,Melkonian, Karin

experimental part, p. 1508 - 1518 (2011/04/24)

Cationic lipids have long been known to serve as antibacterial and antifungal agents. Prior efforts with attachment of cationic lipids to carbohydrate-based surfaces have suggested the possibility that carbohydrate-attached cationic lipids might serve as antibacterial and antifungal pharmaceutical agents. Toward the understanding of this possibility, we have synthesized several series of cationic lipids attached to a variety of glycosides with the intent of generating antimicrobial agents that would meet the requirement for serving as a pharmaceutical agent, specifically that the agent be effective at a very low concentration as well as being biodegradable within the organism being treated. The initial results of our approach to this goal are presented.

Selective preparation of hexakis(6-O-arenesulfonyl)-α-cyclodextrin

Fujita,Ohta,Masunari,Obe,Yamamura

, p. 5519 - 5520 (2007/10/02)

Hexakis(6-O-tosyl)-α-cyclodextrin and hexakis(6-O-(2-naphthalenesulfonyl)-α-cyclodextrin were prepared selectively through the reaction of α-cyclodextrin by use of bis(tributylstannyl) oxide and the corresponding sulfonyl chloride in 32.4 and 77.9%, respectively.

Per-3,6-anhydro-α-cyclodextrin and Per-3,6-anhydro-β-cyclodextrin

Ashton, Peter R.,Ellwood, Paul,Staton, Ian,Stoddart, J. Fraser

, p. 7274 - 7280 (2007/10/02)

The synthesis of the per-3,6-anhydro derivatives of α- and β-cyclodextrins (CDs) is described starting from the corresponding per-6-tosylates.These could only be obtained as pure compounds following repeated HPLC under reversed-phase conditions of the cru

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