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

359761-70-9

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359761-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359761-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,7,6 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 359761-70:
(8*3)+(7*5)+(6*9)+(5*7)+(4*6)+(3*1)+(2*7)+(1*0)=189
189 % 10 = 9
So 359761-70-9 is a valid CAS Registry Number.

359761-70-9Downstream Products

359761-70-9Relevant 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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