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1H-Pyrazole, 5-(2-furanyl)-4,5-dihydro-3-(4-methoxyphenyl)-1-phenyl- is a complex organic compound with the molecular formula C20H17N3O2. It is a derivative of 1H-pyrazole, a five-membered heterocyclic compound containing one nitrogen atom and one hydrogen atom. This specific compound features a 2-furanyl group attached to the 5-position of the pyrazole ring, a 4,5-dihydro structure, a 4-methoxyphenyl group at the 3-position, and a phenyl group at the 1-position. The presence of the methoxy group (-OCH3) on the phenyl ring contributes to its lipophilicity and potential biological activity. 1H-Pyrazole, 5-(2-furanyl)-4,5-dihydro-3-(4-methoxyphenyl)-1-phenyl- may be of interest in the fields of pharmaceuticals and materials science due to its unique structure and potential interactions with biological targets.

4035-37-4

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4035-37-4 Usage

Chemical Class

Pyrazole

Structure

Pyrazole ring fused with a furan ring, methoxyphenyl group, and phenyl group

Pharmacological Properties

Potential use in medicinal chemistry

Biological Activities

Antifungal, antiproliferative, and anti-inflammatory properties

Interest to Researchers

Development of new drugs and therapies

Check Digit Verification of cas no

The CAS Registry Mumber 4035-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,3 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4035-37:
(6*4)+(5*0)+(4*3)+(3*5)+(2*3)+(1*7)=64
64 % 10 = 4
So 4035-37-4 is a valid CAS Registry Number.

4035-37-4Relevant academic research and scientific papers

3-Aryl-5-furylpyrazolines and their biological activities

Cetin, Ahmet,Cansiz,Digrak

, p. 345 - 347 (2007/10/03)

Aryl-furyl substituted pyrazolines 2a-c and 4a-c were prepared by the reaction of α,βunsaturated carbonyl compounds with hydrazine or phenyl hydrazine. N-chloroacetyl derivatives 3a-c were obtained by the N-acetylation of 2a-c. The antibacterial activities of synthesized pyrazolines were examined by employing the disk-diffusion technique. All synthesized compounds showed antibacterial effects in 1200 μg concentration.

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