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2-Pentenoic acid, 5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-5-[(4-methoxyphenyl)methoxy]-, methyl ester, (2E,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

676474-12-7

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676474-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 676474-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,7 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 676474-12:
(8*6)+(7*7)+(6*6)+(5*4)+(4*7)+(3*4)+(2*1)+(1*2)=197
197 % 10 = 7
So 676474-12-7 is a valid CAS Registry Number.

676474-12-7Downstream Products

676474-12-7Relevant academic research and scientific papers

Synthesis of 8-(S)-methoxy-11-desmethyl laulimalide: A novel laulimalide analogue

Gallagher Jr., Brian M.,Zhao, Hongjuan,Pesant, Marc,Fang, Francis G.

, p. 923 - 926 (2007/10/03)

A strategy is outlined which enables preparation of novel laulimalide analogues at C.8 and C.11. A representative analogue, 8-(S)-methoxy-11-desmethyl laulimalide, was synthesized via this route.

LAULIMALIDE ANALOGS AND USES THEREOF

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Page/Page column 121, (2010/02/11)

The present invention provides compounds having formula 1: (I) and pharmaceutically acceptable derivatives thereof, wherein R1-R10, q, t, X0, X1, A, B, D, E, G, J, K, L, M and Z are as described generally and in classes and subclasses herein, and additionally provides pharmaceutical compositions thereof, and methods for the use thereof for the treatment of disorders associated with cellular hyperproliferation.

Synthesis and biological evaluation of (-)-laulimalide analogues

Gallagher Jr., Brian M.,Fang, Francis G.,Johannes, Charles W.,Pesant, Marc,Tremblay, Martin R.,Zhao, Hongjuan,Akasaka, Kozo,Li, Xiang-Yi,Liu, Junke,Littlefield, Bruce A.

, p. 575 - 579 (2007/10/03)

Analogues of the marine natural product (-)-laulimalide were prepared by total synthesis and evaluated in vitro for anticancer activity.

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