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(5-CHLORO-2-HYDROXYPHENYL)(1-PHENYL-1H-PYRAZOL-4-YL)METHANONE is a benzophenone derivative featuring a phenylpyrazole moiety, which positions it as a promising candidate in medicinal chemistry and drug development. Its chemical structure, inclusive of a chlorine atom and a hydroxyl group, indicates potential for interactions with biological targets and enzymes, suggesting possible pharmacological activities.
Used in Pharmaceutical Industry:
(5-CHLORO-2-HYDROXYPHENYL)(1-PHENYL-1H-PYRAZOL-4-YL)METHANONE is used as a potential therapeutic agent for its possible anti-inflammatory and analgesic properties, due to its unique chemical structure that may allow for interactions with biological targets and enzymes.
Further research into the properties and potential uses of (5-CHLORO-2-HYDROXYPHENYL)(1-PHENYL-1H-PYRAZOL-4-YL)METHANONE is warranted to fully explore its capabilities and applications in the field of medicine.

61466-46-4

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61466-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61466-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,6 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61466-46:
(7*6)+(6*1)+(5*4)+(4*6)+(3*6)+(2*4)+(1*6)=124
124 % 10 = 4
So 61466-46-4 is a valid CAS Registry Number.

61466-46-4Relevant academic research and scientific papers

Synthesis and anti-proliferative activity of 4H-chromone based phenylhydrazones, pyrazolecarboxylates and pyrazolylmethanones

Rayala, Nageswara Rao,Kommera, Rajkumar,Cherupally, Dayakar,Thampunuri, Ramalinga Murthy,Shasi, V. Kalivendi,Bhimapaka, China Raju

, p. 34 - 49 (2018/03/29)

Series of 4H-chromone-based hydrazones 3a-z, pyrazolecarboxylates 5a-x and pyrazolylmethanones 6a-u were prepared and screened for their anti-proliferative activity on A549, HeLa, DU145 and MDAMB 231 cell lines. The hydrazone compound 3s with a chloro sub

Hetericyclic Systems. Part 14. Condensation Reactions of 2-(4-Oxo-4H-1-benzopyran-3-yl)-1,3-dioxolane

Ghosh, Chandra Kanta,Bandyopadhyay, Chandrakanta,Morin, Christophe

, p. 1989 - 1994 (2007/10/02)

Nitrogen nucleophiles under 1,4-addition with the title acetal (4; R=H, Me, and Cl) to give an intermediate that ultimately produces in most cases the same product as is obtained from the corresponding aldehyde (3) under similar conditions.Thus, compound

Heterocyclic Systems: Part XIII - Reactions of 3-N,N-Dimethylhydrazonomethyl-, Oximomethyl- and Cyano-chromones with Nucleophiles Containing Nitrogen

Ghosh, Chandra Kanta,Tewari, Nimai,Bandyopadhyay, Chandrakanta

, p. 1200 - 1204 (2007/10/02)

Reactions of the title chromones (3, 9, 10) with nitrogen containing nucleophiles (5-7) have been studied.When treated with phenylhydrazine, the hydrazone (9) produces the same pyrazole 17 (R'=Ph) as obtained by reacting chromone-3-carboxaldehyde (8) with

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