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α-Bromo-4'-nitro-chalcone is a synthetic organic compound characterized by its molecular formula C15H11BrNO3, which indicates the presence of 15 carbon atoms, 11 hydrogen atoms, 1 bromine atom, 1 nitrogen atom, and 3 oxygen atoms. α-bromo-4'-nitro-chalcone features a chalcone structure, which is a type of flavonoid with a carbon-carbon double bond between two aromatic rings. The α-bromo-4'-nitro-chalcone specifically has a bromine atom attached to the alpha carbon of the chalcone structure and a nitro group (-NO2) at the 4' position, which is the carbon adjacent to the carbon bearing the bromine. α-bromo-4'-nitro-chalcone is known for its potential applications in the synthesis of various pharmaceuticals and as a precursor in the preparation of other organic compounds. It is also recognized for its potential biological activities, such as anti-inflammatory and anticancer properties, although further research is needed to fully understand its therapeutic potential.

24374-10-5

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24374-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24374-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24374-10:
(7*2)+(6*4)+(5*3)+(4*7)+(3*4)+(2*1)+(1*0)=95
95 % 10 = 5
So 24374-10-5 is a valid CAS Registry Number.

24374-10-5Relevant academic research and scientific papers

Experimental and Theoretical Study of an Intramolecular CF3-Group Shift in the Reactions of α-Bromoenones with 1,2-Diamines

Muzalevskiy, Vasily M.,Ustynyuk, Yury A.,Gloriozov, Igor P.,Chertkov, Vyacheslav A.,Rulev, Alexander Yu.,Kondrashov, Evgeniy V.,Ushakov, Igor A.,Romanov, Alexey R.,Nenajdenko, Valentine G.

, p. 16982 - 16989 (2015/11/16)

The reactions of trifluoromethylated 2-bromoenones and N,N′-dialkyl-1,2-diamines have been studied. Depending on the structures of the starting compounds, the formation of 2-trifluoroacetylpiperazine or 3-trifluoromethylpiperazine-2-ones was observed. The mechanism of the reaction is discussed in terms of multistep processes involving sequential substitution of bromine in the starting α-bromoenones and intramolecular cyclization of the captodative aminoenones as key intermediates to form the target heterocycles. The results of theoretical calculations are in perfect agreement with the experimental data. The unique role of the trifluoromethyl group in this reaction is demonstrated.

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