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2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-3-(2-furanyl)-, also known as 1-(3,4-dimethoxyphenyl)-3-(2-furanyl)-2-propen-1-one, is a complex organic compound with the molecular formula C13H12O4. It is a derivative of 2-propen-1-one, featuring a 3,4-dimethoxyphenyl group at the 1-position and a 2-furanyl group at the 3-position. 2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-3-(2-furanyl)- is characterized by its unique structure, which combines the properties of an enone with the aromaticity of the dimethoxyphenyl and furanyl moieties. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential applications in the treatment of neurological disorders and as pesticides. The compound's chemical properties, such as reactivity and stability, are influenced by the presence of the electron-donating methoxy groups and the electron-withdrawing carbonyl group, making it a versatile building block in organic synthesis.

4538-04-9

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4538-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4538-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,3 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4538-04:
(6*4)+(5*5)+(4*3)+(3*8)+(2*0)+(1*4)=89
89 % 10 = 9
So 4538-04-9 is a valid CAS Registry Number.

4538-04-9Relevant academic research and scientific papers

Synthesis, cytotoxic properties and tubulin polymerization inhibitory activity of novel 2-pyrazoline derivatives

Abdel-Aziz, Mohamed,Aly, Omar M.,Khan, Sabine S.,Mukherjee, Kamalika,Bane, Susan

scheme or table, p. 535 - 548 (2012/09/08)

A series of novel 1-(3',4',5'-trimethoxybenzoyl)-3,5-diarylpyrazoline derivatives were synthesized and evaluated for their cytotoxic properties on different cancer cell lines and tubulin polymerization inhibitory activity. Compounds 6d and 6e exhibited re

Synthesis and investigation of anti-inflammatory activity and gastric ulcerogenicity of novel nitric oxide-donating pyrazoline derivatives

Shoman, Mai E.,Abdel-Aziz, Mohamed,Aly, Omar M.,Farag, Hassan H.,Morsy, Mohamed A.

scheme or table, p. 3068 - 3076 (2009/10/02)

A group of 3,5-diaryl-2-pyrazoline derivatives were prepared via the reaction of various chalcones with hydrazine hydrate in ethanol. A group of NO-donating-2-pyrazoline derivatives were synthesized by carrying a nitrate ester group or an oxime group onto

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