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(1α,6α,7α,8α)-(+/-)-3-(Phenylsulfonyl)-8-(2-trimethylsilylphenylsulfonyl)tetracyclo<5.1.0.02,4.03,5>octan-6-ol-benzolsulfonat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109552-59-2

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109552-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109552-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,5 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109552-59:
(8*1)+(7*0)+(6*9)+(5*5)+(4*5)+(3*2)+(2*5)+(1*9)=132
132 % 10 = 2
So 109552-59-2 is a valid CAS Registry Number.

109552-59-2Downstream Products

109552-59-2Relevant academic research and scientific papers

Phenylsulphonyl-Substituted Octabisvalenes. - Syntheses and Reactions

Ruecker, Christoph

, p. 1629 - 1644 (2007/10/02)

(Z)-3,7-Bis(phenylsulphonyl)octabisvalene (2), the first derivative of octabisvalene, is synthesized in an eleven-step sequence starting from cis-benzene trioxide.The six new C-C bonds are formed by inter- and intramolecular nucleophilic substitutions at all six C atoms of the starting material.An improved synthesis (shortened to eight steps) yields preparatively useful quantities of 2.Bromine or monovalent nucleophiles add to one of the two bicyclobutane units in 2; the tetracyclo2,4.03,5>octanes of type 32-34, 38-41 obtained do not undergo further addition.Addition to both bicyclobutane systems is achieved intramolecularly by divalent nucleophiles, yielding bridged tricyclo2,4>octanes of type 42/45.Lithation and silylation of 2 as well as reductive removal of the sulphonyl groups give rise to other substituted octabisvalenes (46-54,56), among them to the monosubstituted 3-(phenylsulphonyl)octabisvalene (51).

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