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(3S)-9,10-difluoro-3-methyl-7-oxo-2,3,6,7-tetrahydro-5H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid is a complex chemical compound belonging to the quinoline family, characterized by the presence of fluorine, methyl, oxo, and carboxylic acid functional groups. Its molecular structure features a chiral center at the 3-position, indicated by the (3S) configuration. (3S)-9,10-difluoro-3-methyl-7-oxo-2,3,6,7-tetrahydro-5H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid's potential pharmacological applications are suggested by the diverse biological activities of quinolines, which include antimicrobial, antimalarial, and anticancer properties. The difluoro and methyl substituents on the quinoline ring may modulate the compound's physicochemical properties and biological activity, warranting further research and testing to explore its full potential.

1026952-91-9

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1026952-91-9 Usage

Uses

Used in Pharmaceutical Industry:
(3S)-9,10-difluoro-3-methyl-7-oxo-2,3,6,7-tetrahydro-5H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid is used as a potential pharmaceutical agent for its possible antimicrobial, antimalarial, and anticancer properties. The presence of fluorine and methyl groups may enhance its bioavailability and target specificity, making it a candidate for the development of new drugs to combat resistant infections and cancer.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (3S)-9,10-difluoro-3-methyl-7-oxo-2,3,6,7-tetrahydro-5H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid serves as a valuable compound for studying the structure-activity relationships of quinolines. Its unique functional groups and stereochemistry provide opportunities to investigate the effects of these features on biological activity, potentially leading to the design of more effective and selective therapeutic agents.
Used in Drug Discovery and Development:
(3S)-9,10-difluoro-3-methyl-7-oxo-2,3,6,7-tetrahydro-5H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid is utilized in drug discovery and development processes to identify novel lead compounds with potential therapeutic applications. Its complex molecular structure and the presence of various functional groups make it a promising starting point for the optimization of drug candidates targeting a range of diseases and conditions.
Note: The specific applications and uses mentioned above are hypothetical and based on the general properties of quinolines and the presence of functional groups in the compound. Further research and testing are required to validate these potential uses and to determine the safety and efficacy of (3S)-9,10-difluoro-3-methyl-7-oxo-2,3,6,7-tetrahydro-5H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1026952-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,9,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1026952-91:
(9*1)+(8*0)+(7*2)+(6*6)+(5*9)+(4*5)+(3*2)+(2*9)+(1*1)=149
149 % 10 = 9
So 1026952-91-9 is a valid CAS Registry Number.

1026952-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name PYR253

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

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More Details:1026952-91-9 SDS

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