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1260085-05-9

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1260085-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1260085-05-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,0,8 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1260085-05:
(9*1)+(8*2)+(7*6)+(6*0)+(5*0)+(4*8)+(3*5)+(2*0)+(1*5)=119
119 % 10 = 9
So 1260085-05-9 is a valid CAS Registry Number.

1260085-05-9Relevant academic research and scientific papers

Synthesis and structure-activity relationship of vicenistatin, a cytotoxic 20-membered macrolactam glycoside

Fukuda, Hayato,Nishiyama, Yuko,Nakamura, Shiina,Ohno, Yutaro,Eguchi, Tadashi,Iwabuchi, Yoshiharu,Usui, Takeo,Kanoh, Naoki

supporting information, p. 2872 - 2881 (2013/02/23)

We have developed two syntheses of vicenistatin and its analogues. Our first-generation strategy included the rapid and sequential assembly of the macrocyclic lactam by using an intermolecular Horner-Wadsworth-Emmons reaction between the C3-C13 fragment and the C1-C2, C14-C19 fragment, followed by an intramolecular Stille coupling reaction. The second-generation strategy utilized a ring-closing metathesis of a hexaene intermediate to generate the desired 20-membered macrolactam. This second-generation strategy made it possible to prepare synthetic analogues of vicenistatin, including the C20- and/or C23-demethyl analogues. Evaluation of the cytotoxic effect of these analogues indicated the importance of the fixed conformation of aglycon for determining the biological activity of the vicenistatins. An enantioselective total synthesis of vicenistatin (1) was accomplished by using an intermolecular Horner-Wadsworth-Emmons reaction and a ring-closing metathesis as key steps. This strategy made it possible to prepare synthetic analogues of vicenistatin, including the C20- and/or C23-demethyl vicenistatins. Evaluation of their cytotoxicity indicated the importance of the fixed conformation of aglycon in determining biological activity. Copyright

Concise total synthesis of vicenistatin

Fukuda, Hayato,Nakamura, Shiina,Eguchi, Tadashi,Iwabuchi, Yoshiharu,Kanoh, Naoki

supporting information; experimental part, p. 2589 - 2592 (2010/12/18)

A highly convergent total synthesis of macrocyclic lactam glycoside vicenistatin is described. Key features of the synthesis include rapid assembly of the macrolactam part and macrocyclic ring closure via intramolecular Stille coupling. Georg Thieme Verlag Stuttgart New York.

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