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(11S)-(12Z)-11-dimethoxymethyl-11-ethoxycarbonylmethyl-1,2-dimethoxy-7-(2-nitro-benzenesulfonyl)-6,7,8,9,10,11-hexahydro-5H-7,14-diaza-cycloundeca[a]indene-14-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

545363-06-2

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545363-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 545363-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,5,3,6 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 545363-06:
(8*5)+(7*4)+(6*5)+(5*3)+(4*6)+(3*3)+(2*0)+(1*6)=152
152 % 10 = 2
So 545363-06-2 is a valid CAS Registry Number.

545363-06-2Upstream product

545363-06-2Relevant academic research and scientific papers

Enantioselective total synthesis of aspidophytine

Sumi, Shinjiro,Matsumoto, Koji,Tokuyama, Hidetoshi,Fukuyama, Tohru

, p. 1891 - 1893 (2007/10/03)

(Matrix presented) An enantioselective total synthesis of aspidophytine is described. The indole fragment bearing a cis-alkene substituent was efficiently prepared through radical cyclization of a 2-alkenylphenylisocyanide followed by Sonogashira coupling of the generated 2-iodoindole derivative with a functionalized acetylene unit. After formation of the 11-membered cyclic amine, the aspidosperma skeleton and lactone ring were constructed to complete the total synthesis.

Stereocontrolled total synthesis of (-)-aspidophytine

Sumi, Shinjiro,Matsumoto, Koji,Tokuyama, Hidetoshi,Fukuyama, Tohru

, p. 8571 - 8587 (2007/10/03)

The enantioselective stereocontrolled total synthesis of aspidophytine is described. The key indole intermediate was prepared by radical cyclization of 2-alkenylphenylisocyanide, followed by Sonogashira-coupling with a highly functionalized terminal acetylene. The 11-membered cyclic amine, a precursor for the formation of the aspidosperma skeleton, was synthesized using nitrobenzenesulfonamide chemistry. After construction of the pentacyclic skeleton, the lactone ring was formed to complete the total synthesis.

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