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(-)-(2-phenylbutyl)phenylmethyltin iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96306-49-9

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96306-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96306-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,0 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96306-49:
(7*9)+(6*6)+(5*3)+(4*0)+(3*6)+(2*4)+(1*9)=149
149 % 10 = 9
So 96306-49-9 is a valid CAS Registry Number.

96306-49-9Downstream Products

96306-49-9Relevant academic research and scientific papers

Synthesis of optically active allyltin compounds and their application to enantioselective synthesis of secondary homoallyl alcohols

Otera, Junzo,Yoshinaga, Yukari,Yamaji, Takeshi,Yoshioka, Takakazu,Kawasaki, Yuzuru

, p. 1213 - 1218 (2008/10/08)

Three types of optically active allyltin compounds, R*2Sn(allyl)2 (R* = 2-phenylbutyl, 2-methylbutyl, and 3-phenylbutyl), R*R1Sn(allyl)2 (R* = 2-octyl or 2-phenylbutyl, R1 = phenyl), and R*R1R2Sn(allyl) (R* = 2-phenylbutyl, R1 = phenyl, R2 = methyl), have been synthesized. On the basis of 1H NMR spectra, a π-stacking interaction between the 2-phenylbutyl and the allyl groups is suggested. Optically active allyltin compounds thus obtained were subjected to reaction with aldehydes. Among various allyltin compounds, only diallylbis(2-phenylbutyl)tin exhibits good enantioselectivity. The reaction proceeds through addition of the allyl group on the re face of aldehydes. The mechanism can be accounted for on the basis of a π-stacking interaction between allyl and phenyl groups.

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