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(1S,2S)-1-Benzyloxy-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-4-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111462-27-2

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111462-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111462-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,6 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111462-27:
(8*1)+(7*1)+(6*1)+(5*4)+(4*6)+(3*2)+(2*2)+(1*7)=82
82 % 10 = 2
So 111462-27-2 is a valid CAS Registry Number.

111462-27-2Relevant academic research and scientific papers

Stereoselective total synthesis of (+)-synargentolide A

Prasad, Kavirayani R.,Penchalaiah, Kamala

experimental part, p. 2853 - 2858 (2011/03/18)

The stereoselective synthesis of synargentolide A, a polyhydroxy δ-lactone, has been accomplished from tartaric acid. The key steps in the synthesis involve Keck and Brown allylations and ring closing metathesis.

New Chirons from D-Glucose. Regio- and Diastereoselective C-C Bond Forming Reactions Exploiting Novel Aldotetrafuranose Acetates as Chiral Synthetic Equivalents of Tartaric Aldehydes

Dhavale, Dilip D.,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille

, p. 4100 - 4105 (2007/10/02)

Two differentially protected tetrafuranose acetates 5 and 6 have been prepared from diacetone D-glucose in parallel short routes.They clearly act as chiral synthetic equivalents of D- and meso-tartaric aldehydes when exploited in Lewis acid promoted react

STEREOSELECTIVE ALLYLATION FOR PREPARATION OF L-HEXOSE DERIVATIVES

Williams, D. R.,Klinger, Franz D.

, p. 869 - 872 (2007/10/02)

The reaction of allyltrimethylsilane with α,β-dialkoxyaldehydes is catalyzed by magnesium bromide, and provides for a highly stereoselective allylation which is predicted by α-chelation of the Lewis acid.The observed stereocontrol is opposite to that gene

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