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4-(1,2-diphenylprop-1-en-1-yl)phenol, also known as 4-(1,2-diphenylallyl)phenol, is an organic compound characterized by a phenol group (C6H5OH) with a 1,2-diphenylallyl substituent attached to the para position (4th carbon). The 1,2-diphenylallyl group consists of a propene (allyl) chain with two phenyl rings attached to the first and second carbons, respectively. This molecule is a type of phenolic compound with a conjugated diene system, which can participate in various chemical reactions due to its unsaturated nature. It is often used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structural features and reactivity.

899-24-1

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899-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 899-24-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 899-24:
(5*8)+(4*9)+(3*9)+(2*2)+(1*4)=111
111 % 10 = 1
So 899-24-1 is a valid CAS Registry Number.

899-24-1Downstream Products

899-24-1Relevant academic research and scientific papers

Triphenylethylene analogues: Design, synthesis and evaluation of antitumor activity and topoisomerase inhibitors

Rani, Sudesh,Paul, Kamaldeep

, (2020)

To structurally relate anticancer drug tamoxifen used in the treatment of breast cancer, a sequence of compounds is designed and synthesized as potential drug candidates. McMurry coupling reaction is used as the key synthetic step in the preparation of these analogues and the ratios of E/Z-isomers are determined on the basis of NMR and HPLC experiments. The new compounds are found to be cytotoxic in the micromolar range with 60 human tumor cell lines at one dose and five dose concentration levels. Detailed studies on the most active compounds 11–13 show these compounds are capable to inhibit the growth of cancer cells. Finally, with the aim to correlate the antiproliferative activity with an intracellular target(s), the effect on relaxation activity of DNA topoisomerase-II is assayed. The relevance of interaction of most active compounds with topoisomerase-II is demonstrated which is also supported by docking studies.

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