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N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-3-fluorobenzamide is a complex organic compound with a molecular formula of C18H16FN3O2. It is characterized by a pyrazolone core, which is a heterocyclic ring system consisting of a pyrazole (a five-membered ring with two nitrogen atoms) and a ketone group. The compound features a 3-fluorobenzamide group attached to the pyrazolone, which introduces a fluorine atom to the benzene ring. This fluorination can significantly influence the compound's properties, such as its reactivity, lipophilicity, and potential biological activity. The presence of methyl groups at the 1 and 5 positions of the pyrazolone ring, along with the phenyl group at the 2 position, contributes to the compound's steric and electronic characteristics. This chemical structure suggests potential applications in medicinal chemistry, particularly in the development of new drugs, due to its ability to interact with various biological targets.

2824-15-9

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2824-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2824-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2824-15:
(6*2)+(5*8)+(4*2)+(3*4)+(2*1)+(1*5)=79
79 % 10 = 9
So 2824-15-9 is a valid CAS Registry Number.

2824-15-9Downstream Products

2824-15-9Relevant academic research and scientific papers

Ru-Catalyzed C(sp2)?H Bond Arylation of Benzamides Bearing a Novel 4-Aminoantipyrine as a Directing Group

Al Mamari, Hamad H.,Al Kiumi, Diana,Al Rashdi, Tamadher,Al Quraini, Huda,Al Rashdi, Malak,Al Sheraiqi, Sumayya,Al Harmali, Sara,Al Lamki, Mohammed,Al Sheidi, Ahmed,Al Zadjali, Asma

supporting information, p. 3598 - 3603 (2021/07/22)

A novel design-based removable N,O-bidentate directing group based on cheap and commercially available 4-aminoantipyrine (AAP) is reported. Aromatic AP amides bearing 4-aminoantipyrine underwent efficient Ru-catalyzed C(sp2)?H arylation using [RuCl2(PPh3)3] as a catalyst and aryl bromides as electrophiles. The novel bidentate directing group enabled the C?H functionalization reaction with good scope, good functional group tolerance and in decent yields.

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