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[2-(4-chlorophenyl)-4,5-dioxo-1-(pyridinium-3-ylmethyl)pyrrolidin-3-ylidene][5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl]methanolate is a complex organic compound characterized by its unique structure, which includes a pyrrolidin-3-ylidene core bonded to a 4-chlorophenyl group and a pyridinium-3-ylmethyl group. Additionally, it features a 5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl group and a methanolate group. [2-(4-chlorophenyl)-4,5-dioxo-1-(pyridinium-3-ylmethyl)pyrrolidin-3-ylidene][5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl]methanolate's distinct architecture and properties suggest potential applications in various fields, such as pharmaceuticals, chemistry, and material science. However, further research and analysis are required to explore and confirm its full potential.

5280-10-4

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5280-10-4 Usage

Uses

Used in Pharmaceutical Applications:
[2-(4-chlorophenyl)-4,5-dioxo-1-(pyridinium-3-ylmethyl)pyrrolidin-3-ylidene][5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl]methanolate is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique structure may allow it to interact with specific biological targets, potentially leading to novel therapeutic applications.
Used in Chemical Synthesis:
In the chemical industry, [2-(4-chlorophenyl)-4,5-dioxo-1-(pyridinium-3-ylmethyl)pyrrolidin-3-ylidene][5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl]methanolate may serve as a key intermediate or building block in the synthesis of more complex molecules. Its versatile functional groups could be exploited in various chemical reactions to produce a range of valuable compounds.
Used in Material Science:
[2-(4-chlorophenyl)-4,5-dioxo-1-(pyridinium-3-ylmethyl)pyrrolidin-3-ylidene][5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl]methanolate's structural features and properties might also make it suitable for use in the development of new materials with specific characteristics. For example, it could be employed in the creation of advanced polymers, coatings, or other materials with unique mechanical, electronic, or optical properties.
Used in Research and Development:
Due to its complex structure and potential applications, [2-(4-chlorophenyl)-4,5-dioxo-1-(pyridinium-3-ylmethyl)pyrrolidin-3-ylidene][5-(ethoxycarbonyl)-2,4-dimethyl-1H-pyrrol-3-yl]methanolate may be utilized in academic and industrial research settings. It could serve as a model compound for studying various chemical and biological phenomena, as well as for testing new synthetic methods and techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 5280-10-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5280-10:
(6*5)+(5*2)+(4*8)+(3*0)+(2*1)+(1*0)=74
74 % 10 = 4
So 5280-10-4 is a valid CAS Registry Number.

5280-10-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,8-trifluoroquinoline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5280-10-4 SDS

5280-10-4Relevant academic research and scientific papers

HETEROARYL COMPOUNDS AS CXCR4 INHIBITORS, COMPOSITION AND METHOD USING THE SAME

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Paragraph 00294-00296, (2019/04/16)

The present disclosure provides heteroaryl compounds of Formula (I), processes for their preparation, pharmaceutical compositions containing them, and their use in the treatment of diseases and disorders, arising from or related to the CXCR4 pathway.

Reaction of quinolines fluorinated at the benzene ring with nitrogen-centered nucleophiles

Safina,Selivanova,Bagryanskaya,Shteingarts

experimental part, p. 1049 - 1061 (2010/10/04)

A primary functionalization of quinolines polyfluorinated at the benzene ring (5, 7-difluoro-, 5, 7, 8-trifluoro-, 5, 6, 8-trifluoro-, 8-chloro-5, 7-difluoro-, 5, 6, 7, 8-tetrafluoro-, and 5, 7, 8-trifluoro-6-(trifluoromethyl) quinolines) by the reaction

Effects of oligofluorine substitution on the mutagenicity of quinoline: A study with twelve fluoroquinoline derivatives

Kato, Taka-Aki,Saeki, Ken-Ichi,Kawazoe, Yutaka,Hakura, Atsushi

, p. 149 - 157 (2007/10/03)

A total of 12 variously fluorinated derivatives of quinoline (Q) were tested for their mutagenicity in Salmonella typhimurium TA100 in the presence of S9 mix to investigate the structure-mutagenicity relationship in oligofluorinated quinolines. Nine of th

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