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(2E,6E,8E)-(4R,5R,10S,11R,12S)-11-(4-Methoxy-benzyloxy)-2,4,6,8,10,12-hexamethyl-5-triisopropylsilanyloxy-docosa-2,6,8-trienoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

443304-99-2

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  • (2E,6E,8E)-(4R,5R,10S,11R,12S)-11-(4-Methoxy-benzyloxy)-2,4,6,8,10,12-hexamethyl-5-triisopropylsilanyloxy-docosa-2,6,8-trienoic acid ethyl ester

    Cas No: 443304-99-2

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  • (2E,6E,8E)-(4R,5R,10S,11R,12S)-11-(4-Methoxy-benzyloxy)-2,4,6,8,10,12-hexamethyl-5-triisopropylsilanyloxy-docosa-2,6,8-trienoic acid ethyl ester

    Cas No: 443304-99-2

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443304-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443304-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,3,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 443304-99:
(8*4)+(7*4)+(6*3)+(5*3)+(4*0)+(3*4)+(2*9)+(1*9)=132
132 % 10 = 2
So 443304-99-2 is a valid CAS Registry Number.

443304-99-2Relevant articles and documents

Efficient total synthesis of khafrefungin: Convergent approach using Suzuki coupling under thallium-free conditions toward multigram-scale synthesis

Mori, Yuichiro,Nakamura, Masayuki,Wakabayashi, Takeshi,Mori, Kouhei,Kobayashi, Shu

, p. 601 - 603 (2002)

An efficient and practical synthetic route to khafrefungin, an antifungal agent, has been developed based on successive coupling of three components, 3, 4, and then 2. A key step of the synthesis is the Suzuki coupling of 2 and 10, in which the use of tox

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