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2A,2B-O,O-di(mesitylenesulfonyl)-Sb-cyclodextrine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

189871-93-0

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189871-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189871-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,8,7 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 189871-93:
(8*1)+(7*8)+(6*9)+(5*8)+(4*7)+(3*1)+(2*9)+(1*3)=210
210 % 10 = 0
So 189871-93-0 is a valid CAS Registry Number.

189871-93-0Downstream Products

189871-93-0Relevant articles and documents

The first hetero-bifunctionalization of the secondary face of β-cyclodextrin: Selective and efficient conversion of the A-ring of a 2A,2B-disulfonate to 2A,3A- epoxymannoside

Fukudome, Makoto,Sugimoto, Yuji,Yuan, De-Qi,Fujita, Kahee

, p. 3168 - 3170 (2008/02/12)

The A-ring of 2A,2B-O,O-di(mesitylenesulfonyl)- β-cyclodextrin was converted to 2A,3A-epoxymannoside without affecting the other sulfonylated residue, which affords the first approach to hetero-bifunctionalizati

Preparation of di-altro-β-cyclodextrins with two altrosides as the macrocyclic units through selective synthesis of regioisomers of di(2-O- mesitylenesulfonyl)-β-cyciodextrin

Ohta, Kazuko,Fujita, Kahee,Shimada, Hideaki,Ikegami, Yoshihiro,Nogami, Yasuyoshi,Koga, Toshitaka

, p. 631 - 635 (2007/10/03)

Regioisomers of di(2-O-mesitylenesulfonyl)-β-cyclodextrin 2-4 were synthesized in 3, 4 times larger yields compared to those of the reported method using dibutyltin oxide/triethylamine/p-toluenesulfonyl chloride. Regio-isomers of di-mannoepoxy-β-cyclodextrin 5-7 were prepared from 2-4 and converted to the corresponding di-altro-β-cyclodextrins (8-10) with two altrosides as macrocyclic units, respectively. Conformations of the altrose parts of di-altro-β-cyclodextrins were investigated by NMR, and the altroside was found to change its conformation depending on whether or not it is a member of the macrocyclic ring and its position in the ring.

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