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1-Piperidinecarboxylic acid, 4-[[[4-(2-fluoro-4-nitrophenoxy)-6-methoxy-7-quinolinyl]oxy]methyl]-, 1,1-dimethylethyl ester is a complex organic compound derived from piperidinecarboxylic acid. It features a unique structure with quinoline and piperidine groups, as well as a 4-[[[4-(2-fluoro-4-nitrophenoxy)-6-methoxy-7-quinolinyl]oxy]methyl]group and a 1,1-dimethylethyl ester modification. 1-Piperidinecarboxylic acid,
4-[[[4-(2-fluoro-4-nitrophenoxy)-6-methoxy-7-quinolinyl]oxy]methyl]-,
1,1-dimethylethyl ester holds potential as a bioactive molecule with applications in medicinal chemistry.

849217-45-4

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849217-45-4 Usage

Uses

Used in Pharmaceutical Industry:
1-Piperidinecarboxylic acid, 4-[[[4-(2-fluoro-4-nitrophenoxy)-6-methoxy-7-quinolinyl]oxy]methyl]-, 1,1-dimethylethyl ester is used as a potential drug candidate for the treatment of certain diseases or conditions due to its unique structure and bioactivity. The presence of quinoline and piperidine groups in its composition suggests that it may have therapeutic properties that can be further explored and developed.
Further research and testing are required to fully understand the potential uses and effects of 1-Piperidinecarboxylic acid, 4-[[[4-(2-fluoro-4-nitrophenoxy)-6-methoxy-7-quinolinyl]oxy]methyl]-, 1,1-dimethylethyl ester in the pharmaceutical industry. Its complex structure and the presence of various functional groups indicate that it may have specific interactions with biological targets, making it a promising candidate for drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 849217-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,2,1 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849217-45:
(8*8)+(7*4)+(6*9)+(5*2)+(4*1)+(3*7)+(2*4)+(1*5)=194
194 % 10 = 4
So 849217-45-4 is a valid CAS Registry Number.

849217-45-4Relevant academic research and scientific papers

Preparation method of aryloxy quinoline compound

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Paragraph 0059; 0067-0071; 0092-0094; 0101-0103; 0110-0112, (2021/04/29)

The invention provides a preparation method of an aryloxy quinoline compound, and particularly provides a method for preparing an aryloxy quinoline compound with a structure shown in a formula (I) by taking 4-chloro-6-methoxy-7-quinolinol as a starting ra

Met kinase inhibitors

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Page/Page column 17, (2010/11/26)

The present invention is directed to compounds that are useful for treating cancer having one of the following Formulas:

C-MET MODULATORS AND METHODS OF USE

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, (2010/11/24)

The present invention provides compounds, which have activity for modulating protein kinase enzymatic activity and are potentially useful for modulating cellular activities such as, e.g., proliferation, differentiation, programmed cell death, migration and chemoinvasion. The present invention also provides compositions containing such compounds, and methods for producing and using such compounds and compositions.

C-MET MODULATORS AND METHODS OF USE

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, (2008/06/13)

The present invention provides compounds for modulating protein kinase enzymatic activity for modulating cellular activities such as proliferation, differentiation, programmed cell death, migration and chemoinvasion. More specifically, the invention provides quinazolines and quinolines which inhibit, regulate and/or modulate kinase receptor, particularly c-Met, KDR, c-Kit, flt-3 and flt-4, signal transduction pathways related to the changes in cellular activities as mentioned above, compositions which contain these compounds, and methods of using them to treat kinase-dependent diseases and conditions. The present invention also provides methods for making compounds as mentioned above, and compositions which contain these compounds.

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