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ethyl 4,9-dimethyl-2-oxo-2H-furo-[2,3-h]chromene-8-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20052-02-2

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20052-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20052-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,5 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20052-02:
(7*2)+(6*0)+(5*0)+(4*5)+(3*2)+(2*0)+(1*2)=42
42 % 10 = 2
So 20052-02-2 is a valid CAS Registry Number.

20052-02-2Downstream Products

20052-02-2Relevant academic research and scientific papers

Conventional and microwave-assisted syntheses and solid-state structure of new coumarins and angelicins

Hejchman, Elzbieta,Trykowska Konc, Joanna,MacIejewska, Dorota,Kruszewska, Hanna

, p. 2392 - 2402 (2011)

New derivatives of coumarin and angelicin, 8-acetyl-7-cyanomethoxy-4- methyl-chromen-2-one (1), 8-acetyl-7-ethoxycarbonylmethoxy-4-methyl-chromen-2- one (2), 8-cyano-4,9-dimethyl-2H-furo[2,3-h]-1-chromen-2-one (3), and 8-ethoxycarbonyl-4,9-dimethyl-(2H-furo[2,3-h]-1-chromen-2-one) (4) were obtained by conventional synthesis and by efficient and high-yielding microwave-assisted synthesis. The solid structures were analyzed using 13C cross polarization/magic angle spinning (CP/MAS) NMR spectroscopy. Compounds 1 and 3 were evaluated for potential anticancer activity in an in vitro screening panel of 60 human tumor cell lines. Selected leukemia, non-small-cell lung, and renal cancer lines showed promising sensitivity to these compounds. Additionally, compound 4 was shown to inhibit growth of Gram-positive strains.

New synthesis of 8-alkoxycarbonylangelicins

Tolmachev,Podkhalyuzina,Kuznetsova,Traven'

, p. 1008 - 1012 (2007/10/03)

A new procedure was developed for the synthesis of 8-alkoxycarbonylangelicins by base-catalyzed cyclization of ortho-acyl(hydroxy)coumarins with haloacetic acid esters. The procedure was successfully applied to prepare a series of new 8-alkoxycarbonyl-and 8-acylangelicins.

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