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(4R,5S)-2-[2-(benzyloxy)ethyl]-5-fluoro-4,6-bis(triisopropylsilyloxy)-1-hexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1020727-65-4

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1020727-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1020727-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,7,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1020727-65:
(9*1)+(8*0)+(7*2)+(6*0)+(5*7)+(4*2)+(3*7)+(2*6)+(1*5)=104
104 % 10 = 4
So 1020727-65-4 is a valid CAS Registry Number.

1020727-65-4Relevant academic research and scientific papers

Catalytic asymmetric synthesis and anticancer effects of the novel non-calcemic analog of vitamin D, 2α-fluoro-19-nor-22-oxa-1α,25-dihydroxyvitamin D3 in metastatic lung carcinoma

Nakagawa, Kimie,Okano, Toshio,Ozono, Keiichi,Kato, Shigeaki,Kubodera, Noboru,Ohba, Shiho,Itoh, Yoshimitsu,Mikami, Koichi

, p. 654 - 667 (2008/01/06)

1α,25-Dihydroxyvitamin D3 (1α,25-D3) has potent antiproliferative and anti-invasive properties in vitro in cancer cells. However, the major limitation to its clinical use is that it causes hypercalcemia. Therefore, vitamin D analogs with potent cell regulatory effects but with weaker calcemic effects than 1α,25-D3 are required. Among them, 22-oxa-1α,25-D3 and 19-nor-1α,25-D3 have anti-cancer effects with relatively low calcemic effects. Modifications at the C-2α position of the A-ring also produced analogs with a unique biological profile. Not only the side-chain but also the A-ring modification thus generates a unique analog with potent cell regulatory effects and low calcemic activity as well. We report here that the hybrid 1α,25-D3 analog, synthesized via the highly regio- and stereo-selective ring opening 2α-fluorination and catalytic asymmetric carbonyl-ene cyclization, with 2α-fluoro, 19-nor, and 22-oxa modification exhibits unique cell regulatory activities against the development of metastatic lung carcinoma.

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