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4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenylamine is a complex organic molecule with a molecular formula C16H10ClFN3O. It features a fluorophenylamine group connected to a pyrrolopyridine ring, which is substituted with a chlorine atom. 4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenylamine's structural characteristics, including its aromatic rings and amine functional group, are commonly found in pharmaceuticals and bioactive compounds. The chlorine and fluorine atoms present in the molecule offer potential sites for further chemical modification, which could enhance its pharmacological properties.

688781-89-7

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688781-89-7 Usage

Uses

Used in Pharmaceutical Applications:
4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenylamine is used as a potential pharmaceutical compound for its structural characteristics that are commonly found in drugs and bioactive molecules. The presence of aromatic rings and an amine functional group, along with the chlorine and fluorine atoms, suggests that {4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenyl}amine may have applications in the development of new medications.
Used in Chemical Modification:
In the field of medicinal chemistry, 4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenylamine is used as a starting material for chemical modifications. The chlorine and fluorine atoms in the molecule provide opportunities for further functionalization, which could lead to the development of compounds with improved pharmacological properties.
Used in Research and Development:
4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenylamine is also used in the research and development of new pharmaceuticals. The exploration of its potential uses and properties in the pharmaceutical field requires further investigation, which can contribute to the advancement of drug discovery and development processes.
Used in Drug Design and Synthesis:
In the drug design industry, 4-[(6-chloro-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenylamine is used as a key intermediate in the synthesis of novel drug candidates. Its unique structure and functional groups make it a valuable building block for creating new molecules with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 688781-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,7,8 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 688781-89:
(8*6)+(7*8)+(6*8)+(5*7)+(4*8)+(3*1)+(2*8)+(1*9)=247
247 % 10 = 7
So 688781-89-7 is a valid CAS Registry Number.

688781-89-7Relevant academic research and scientific papers

Efficient synthesis of 4-O- and C-substituted-7-azaindoles

Figueroa-Pérez, Santiago,Bennabi, Samir,Schirok, Hartmut,Thutewohl, Michael

, p. 2069 - 2072 (2007/10/03)

6-Chloro-4-nitro- and 4,6-dichloro-1H-pyrrolo[2,3-b]pyridine are versatile building blocks that allow the synthesis of 4-substituted 7-azaindole derivatives by simple nucleophilic displacement of the 4-substituent. Herein, we report on their reaction with

HETARYLOXY-SUBSTITUTED PHENYLAMINO PYRIMIDINES AS RHO KINASE INHIBITORS

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Page/Page column 23-24, (2010/02/14)

The invention relates to hetaryloxy-substituted phenylamino pyrimidines, a method for the production thereof, and the use thereof for producing medicaments utilized for the treatment and/or prevention of diseases in humans and animals, particularly cardiovascular diseases.

HETEROARYLOXY-SUBSTITUTED PHENYLAMINOPYRIMIDINES AS RHO-KINASE INHIBITORS

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, (2010/02/06)

The invention relates to heteroaryloxy-substituted phenylaminopyrimidines, to methods for the production thereof, and to the use of the same for producing medicaments for the treatment and/or prophylaxis of diseases, especially cardiovascular diseases. The inventive compounds inhibit Rho-kinase.

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