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6-chloro-3-(4-methoxy-phenyl)-2-phenyl-3H-quinazolin-4-one is a complex organic compound belonging to the quinazolinone class. It features a quinazolinone core structure, with a 6-chloro substituent, a 4-methoxy-phenyl group, and a phenyl group attached to the 3-position. 6-chloro-3-(4-methoxy-phenyl)-2-phenyl-3H-quinazolin-4-one is characterized by its unique molecular structure, which may exhibit various biological activities and potential applications in pharmaceutical research. Its chemical formula is C21H16ClNO3, and it has a molecular weight of 369.8 g/mol. 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 investigation in the field of medicinal chemistry.

7079-14-3

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7079-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7079-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7079-14:
(6*7)+(5*0)+(4*7)+(3*9)+(2*1)+(1*4)=103
103 % 10 = 3
So 7079-14-3 is a valid CAS Registry Number.

7079-14-3Downstream Products

7079-14-3Relevant academic research and scientific papers

Synthesis and evaluation of fused pyrimidine derivatives as anti-inflammatory, antiproliferative and antimicrobial agents

Vachala, Seekarajapuram Dinakaran,Srinivasan, Keloth Kothari,Prakash, Peralam Yegneswaran

, p. 2998 - 3005 (2012/10/30)

In this study, condensation of 2-amino-5-chlorobenzoic acid with benzoyl chloride afforded 2-benzamido-5- chloro benzoic acid which on cyclization with different primary amines yielded the corresponding 6-chloro-2-phenyl- 3-substituted quinazolin-4(3H)-ones (V1-V8). The reaction was monitored by thin layer chromatographic analysis. The structure of the synthesized compounds was confirmed by spectral studies and elemental analysis. All these compounds were screened for their anti-inflammatory, antiproliferative and antimicrobial activities. Anti-inflammatory activity was done by rat paw oedema method. Compounds V6 and V5 showed a good percentage inhibition of inflammation at the 2nd and the 3rd h, respectively. Antiproliferative activity was carried out byMTT assay againstChang liver,Hep2 andHeLa cell lines. Compounds V1, V5 and V8 showed antiproliferative activity at low concentrations. The minimum inhibitory concentrations (MIC) of the synthesized compounds against Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli, Candida albicans and Aspergillus flavus was studied by microdilution assay. Compound V4 was found to be a potent antimicrobial agent against the organisms tested. Further, itwas selected for time kill study. These data revealed that the compounds containing chloro- and/or fluoro-substituted phenyl ring or N,N-dimethyl ethyl substitutions in the quinazolin-4(3H)-ones led to increase of their biological activities. Springer Science+Business Media, LLC 2011.

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