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5-(2-fluoro-phenyl)-3-methyl-isoxazole-4-carboxylic acid is a complex organic compound with the molecular formula C12H8FNO3. It is characterized by a 2-fluoro-phenyl group attached to the 5-position of an isoxazole ring, which also features a methyl group at the 3-position and a carboxylic acid group at the 4-position. 5-(2-fluoro-phenyl)-3-methyl-isoxazole-4-carboxylic acid is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its unique structure allows it to interact with biological targets, making it a valuable component in the development of new therapeutic agents. The compound's properties, such as its fluorine substitution, can influence its reactivity, lipophilicity, and binding affinity to proteins, which are critical factors in drug design.

1736-23-8

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1736-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1736-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1736-23:
(6*1)+(5*7)+(4*3)+(3*6)+(2*2)+(1*3)=78
78 % 10 = 8
So 1736-23-8 is a valid CAS Registry Number.

1736-23-8Downstream Products

1736-23-8Relevant academic research and scientific papers

Design, synthesis and cytotoxic activities of scopoletin-isoxazole and scopoletin-pyrazole hybrids

Shi, Wei,Hu, Jinglin,Bao, Na,Li, Dongang,Chen, Li,Sun, Jianbo

, p. 147 - 151 (2016/12/27)

12 novel scopoletin-isoxazole and scopoletin-pyrazole hybrids were designed, synthesized and their chemical structures were confirmed by HR-MS, IR,1H NMR and13C NMR spectra. The anticancer activities of the newly synthesized compounds were evaluated in vitro against three human cancer cell lines including HCT-116, Hun7 and SW620 by MTT assay. The screening results showed that six compounds (9a, 9c, 9d, 12a, 18b and 18d) exhibited potent cytotoxic activities with IC50values below 20?μM. Besides, we have further evaluated the growth inhibitory activities of six compounds against the human normal tissue cell lines HFL-1. Especially, compound 9d displayed significant anti-proliferative activity with IC50values ranging from 8.76?μM to 9.83?μM and weak cytotoxicity with IC50value of 90.9?μM on normal cells HFL-1, which suggested that isoxazole-based hybrids of scopoletin were an effective chemical modification to improve the anticancer activity of scopoletin.

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