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7-fluoro-2-(4-methoxy-phenyl)-chromen-4-one is a chemical compound with the molecular formula C16H11FO3. It is a derivative of the chromen-4-one class of compounds, characterized by the presence of a fluorine atom at the 7th position and a 4-methoxy-phenyl group at the 2nd position. 7-fluoro-2-(4-methoxy-phenyl)-chromen-4-one is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. Its structure features a chromene ring system, which is a type of heterocyclic compound with a benzene ring fused to a pyran ring. The 4-methoxy group provides additional functionality and can influence the compound's reactivity and biological activity. The compound's properties, such as solubility and stability, can be influenced by the presence of these functional groups, making it a subject of interest for further chemical and pharmacological studies.

3915-32-0

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3915-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3915-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3915-32:
(6*3)+(5*9)+(4*1)+(3*5)+(2*3)+(1*2)=90
90 % 10 = 0
So 3915-32-0 is a valid CAS Registry Number.

3915-32-0Downstream Products

3915-32-0Relevant academic research and scientific papers

A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase-B inhibitors

Chimenti, Franco,Fioravanti, Rossella,Bolasco, Adriana,Chimenti, Paola,Secci, Daniela,Rossi, Francesca,Yá?ez, Matilde,Orallo, Francisco,Ortuso, Francesco,Alcaro, Stefano,Cirilli, Roberto,Ferretti, Rosella,Sanna, M. Luisa

experimental part, p. 1273 - 1279 (2010/04/24)

A new series of synthetic flavones, thioflavones, and flavanones has been synthesized and evaluated as potential inhibitors of monoamine oxidase isoforms (MAO-A and -B). The most active series is the flavanone one with higher selective inhibitory activity against MAO-B. Some of these flavanones (mainly the most effective) have been separated and tested as single enantiomers. In order to investigate the MAOs recognition of the most active and selective compounds, a molecular modeling study has been performed using available Protein Data Bank (PDB) structures as receptor models for docking experiments.

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