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86272-41-5

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86272-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86272-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86272-41:
(7*8)+(6*6)+(5*2)+(4*7)+(3*2)+(2*4)+(1*1)=145
145 % 10 = 5
So 86272-41-5 is a valid CAS Registry Number.

86272-41-5Relevant academic research and scientific papers

Asymmetric organocatalytic oxy-Michael addition of alcohols to α,β-unsaturated aldehydes

Kano, Taichi,Tanaka, Youhei,Maruoka, Keiji

, p. 8658 - 8664 (2007)

A 1,4-addition of alcohols to α,β-unsaturated aldehydes was found to be efficiently promoted by biphenyldiamine-based catalyst 3?without formation of the acetals. An asymmetric variant of this reaction has also been performed by designing a novel axially

1,3-Asymmetric Induction in Diastereoselective Allylations of Chiral N-Tosyl Imines

Fettinger, James C.,Gutierrez, David A.,Lo, Anna,Shaw, Jared T.,Toth-Williams, Garrett

, (2022/02/07)

Lewis acid mediated allylations of β-alkoxy N-tosyl imines using allyltrimethylsilane lead to 3-alkoxy homoallylic N-tosyl amines with anti-selectivity. Two methods of Cu(OTf)2-mediated allylations are reported herein, demonstrating that diastereoselectiv

Organocatalytic oxy-Michael addition of alcohols to α,β-unsaturated aldehydes

Kano, Taichi,Tanaka, Youhei,Maruoka, Keiji

, p. 3039 - 3041 (2007/10/03)

1,4-Addition of alcohols to α,β-unsaturated aldehydes was found to be efficiently promoted by biphenyldiamine-based catalyst 3 without formation of the acetals.

Concentration effects in chelation controlled reactions

Springer,Springer, James B.,DeBoard,Deboard, Julie,Corcoran,Corcoran, Robert C.

, p. 8733 - 8736 (2007/10/02)

The diastereoselectivities of addition reactions of allyltrimethylsilane to an α-benzyloxyaldehyde were found to be relatively insensitive to the amount of added TiCl4, and to the absolute concentration of the 1:1 aldehyde/TiCl4 complex. In contrast, diastereoselectivities of similar additions to a structurally related β-benzyloxyaldehyde were highly dependent on these variables.

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