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(13R,19R,20R)-3-(3'-acetoxypropyl)-19-(4'-benzyloxyphenyl)-13-methoxycarbonylmethyl-8-(2'-nitrobenzenesulfonyl)-2-oxo-18-oxa-3,8,12-triazatricyclo[12.5.2.00.0]heneicosa-14(21),15,17(20)-triene-12-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

566202-84-4

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566202-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 566202-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,6,2,0 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 566202-84:
(8*5)+(7*6)+(6*6)+(5*2)+(4*0)+(3*2)+(2*8)+(1*4)=154
154 % 10 = 4
So 566202-84-4 is a valid CAS Registry Number.

566202-84-4Upstream product

566202-84-4Relevant academic research and scientific papers

Total synthesis of (-)-ephedradine A: An efficient construction of optically active dihydrobenzofuran-ring via C-H insertion reaction

Kurosawa, Wataru,Kobayashi, Hideki,Kan, Toshiyuki,Fukuyama, Tohru

, p. 9615 - 9628 (2007/10/03)

The stereocontrolled total synthesis of (-)-ephedradine A (1) has been accomplished. Construction of optically active dihydrobenzofuran-ring was performed by a novel asymmetric C-H insertion reaction. After an intramolecular ester-amide exchange reaction and a Sharpless asymmetric aminohydroxylation reaction, construction of the complex macrocyclic ring was performed by Ns-strategy and an intramolecular aza-Wittig reaction. Graphical Abstract.

Stereocontrolled total synthesis of (-)-ephedradine a (orantine)

Kurosawa, Wataru,Kan, Toshiyuki,Fukuyama, Tohru

, p. 8112 - 8113 (2007/10/03)

The stereocontrolled total synthesis of (-)-ephedradine A has been accomplished. The synthesis features an asymmetric C-H insertion reaction, an intramolecular ester-amide exchange reaction, and a Sharpless asymmetric aminohydroxylation reaction. Construction of the complex macrocyclic ring was performed by Ns-strategy and an intramolecular aza-Wittig reaction. Copyright

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