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2-Cyclopentene-1-acetaldehyde, 2-formyl-3-methyl-, (S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

203508-76-3

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203508-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203508-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,5,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 203508-76:
(8*2)+(7*0)+(6*3)+(5*5)+(4*0)+(3*8)+(2*7)+(1*6)=103
103 % 10 = 3
So 203508-76-3 is a valid CAS Registry Number.

203508-76-3Downstream Products

203508-76-3Relevant academic research and scientific papers

Centrifugal partition chromatography: An efficient tool to access highly polar and unstable synthetic compounds on a large scale

Markovi, Dean,Barboux, Cdric,Salle De Chou, Ys,Bettach, Judith,Grougnet, Raphal,Deguin, Brigitte

, p. 63254 - 63259 (2014)

Centrifugal partition chromatography (CPC) is an efficient method adaptable for the purification of synthetic compounds with chemical value, significantly simplifying the reaction work-up. From Aucuba japonica Thunb., an abundant natural terpenoid, aucubin, was isolated. Its reduced derivatives and corresponding unstable aglucons were purified by CPC. The latter chiral synthons were obtained under protecting group free conditions using eco-friendly, non-chlorinated solvents and without silica gel.

Crossed intramolecular rauhut-currier-type reactions via dienamine activation

Marques-Lopez, Eugenia,Herrera, Raquel P.,Marks, Timo,Jacobs, Wiebke C.,Koenning, Daniel,De Figueiredo, Renata M.,Christmann, Mathias

supporting information; experimental part, p. 4116 - 4119 (2009/12/06)

The intramolecular Rauhut-Currier reaction creates a carbon-carbon bond between two tethered Michael acceptors. Previous asymmetric versions have relied on 1,4-additions of chiral nucleophilic catalysts. Herein, we Investigate a novel strategy that involves the formation of electron rich dienamines as key Intermediates. Our methodology provides an efficient entry to the iridoid framework.

Synthesis and absolute configuration of rotundial, a mosquito repellent from the leaves of vitex rotundiforia

Takikawa, Hirosato,Yamazaki, Yuichiro,Mori, Kenji

, p. 229 - 232 (2007/10/03)

The enantiomers of rotundial (1), a mosquito repellent from the leaves of Vitex rotundiforia, were synthesized from the enantiomers of limonene oxide (2). The absolute configuration of natural rotundial was determined to be R.

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