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The chemical compound "2H-1-Benzopyran-2-one, 3-[4,5-dihydro-5-(4-methoxyphenyl)-1-phenyl-1H-pyrazol-3-yl]-4-hydroxy-" is a complex organic molecule with a molecular formula of C23H19NO5. It belongs to the class of compounds known as chromones, which are derivatives of benzopyran-2-ones. This specific compound features a pyrazol-3-yl group attached to the chromone core, with a 4-methoxyphenyl and a phenyl substituent on the pyrazole ring. The 4-hydroxy group on the chromone ring indicates the presence of a hydroxyl functional group, which can participate in various chemical reactions and interactions. This molecule is characterized by its potential biological activities and may be of interest in the fields of pharmaceuticals and organic chemistry due to its unique structure and potential applications.

2748-28-9

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2748-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2748-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2748-28:
(6*2)+(5*7)+(4*4)+(3*8)+(2*2)+(1*8)=99
99 % 10 = 9
So 2748-28-9 is a valid CAS Registry Number.

2748-28-9Downstream Products

2748-28-9Relevant academic research and scientific papers

Quantitative photooxidation of 4-hydroxy-3-pyrazolinylcoumarins to pyrazolyl derivatives

Traven, Valery F.,Ivanov, Ivan V.,Pavlov, Aleksandr S.,Manaev, Aleksandr V.,Voevodina, Irina V.,Barachevskii, Valery A.

, p. 345 - 346 (2007)

4-Hydroxy-3-pyrazolinylcoumarins undergo quantitative photooxidation to pyrazolyl derivatives under illumination with visible light at room temperature in a carbon tetrachloride solution.

Synthesis and structure of new 3-pyrazolinylcoumarins and 3-pyrazolinyl-2-quinolones

Traven,Manaev,Voevodina,Okhrimenko

experimental part, p. 1508 - 1515 (2009/10/01)

The reactions of substituted 3-cinnamoyl-4-hydroxycoumarins and 3-cinnamoyl-4-hydroxy-2-quinolones with different phenylhydrazines gave 3-hetaryl-1H-4,5-dihydropyrazoles. The product structures were studied by 1H NMR spectroscopy and mass spect

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