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1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid is a complex chemical compound that belongs to the fluoroquinolone class of antibiotics. It features a naphthyridine core, a piperazine ring, and multiple fluorine and carbonyl groups, which contribute to its antimicrobial activity. 1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid may offer a new and effective solution for the treatment of various bacterial infections.

100490-19-5

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  • 1,8-Naphthyridine-3-carboxylicacid, 1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-

    Cas No: 100490-19-5

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  • 1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid

    Cas No: 100490-19-5

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100490-19-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid is used as an antibiotic agent for the treatment of bacterial infections. Its unique chemical structure and properties provide it with the potential to be a new and effective option in combating resistant bacterial strains.
Used in Research and Development:
In the field of microbiology and pharmaceutical research, 1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid serves as a valuable compound for studying its antimicrobial properties and mechanisms of action. This research can lead to the development of new antibiotics and a better understanding of bacterial resistance.
Used in Clinical Trials:
As a potential new antibiotic, 1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid may be utilized in clinical trials to evaluate its safety, efficacy, and optimal dosage for treating specific bacterial infections. These trials are crucial for determining its suitability as a new therapeutic option in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 100490-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,9 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100490-19:
(8*1)+(7*0)+(6*0)+(5*4)+(4*9)+(3*0)+(2*1)+(1*9)=75
75 % 10 = 5
So 100490-19-5 is a valid CAS Registry Number.

100490-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-difluorophenyl)-6-fluoro-4-oxo-7-piperazin-1-yl-1,8-naphthyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,8-Naphthyridine-3-carboxylicacid,1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)

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:100490-19-5 SDS

100490-19-5Downstream Products

100490-19-5Relevant articles and documents

NOVEL METHOD OF SYNTHESIS OF FLUOROQUINOLONES

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Page/Page column 6; 10-11, (2009/04/24)

The invention relates to a method of preparation of fluoroquinolones of formula (I) from compounds of formula (II): in which R1, R2, R3, R4, R5, R6, R7, and X are as defined in Claim 1.

RIFAMYCIN DERIVATIVES EFFECTIVE AGAINST DRUG-RESISTANT MICROBES

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Page/Page column 38-39, (2010/02/13)

Rifamycin derivatives having antimicrobial activities, including activities against drug-resistant microorganisms are claimed in this invention. The inventive rifamycin derivatives are uniquely designed in that they have a rifamycin moiety covalently linked to a linker group through the C-3 carbon of the rifamycin moiety and the linker is, in turn covalently linked to a therapeutic moiety or antibacterial agent/pharmacophore. The therapeutic moiety can be a quinolone, an oxazolidinone, a macrolide, an aminoglycoside, a tetracycline core or a structure/pharmacophore associated with an antibacterial agent.

Naphthyridine antibacterial compounds

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, (2008/06/13)

Naphthyridine compounds having the formula: STR1 wherein Z is an amine or an aliphatic heterocyclic group, R is a phenyl group or an aromatic heterocyclic group and R1 is hydrogen or a carboxy protecting group. The compounds of the invention ha

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