Welcome to LookChem.com Sign In|Join Free
  • or
1,8-Naphthyridine-3-carboxylic acid, 6-fluoro-1-(4-fluorophenyl)-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo- , ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100546-84-7

Post Buying Request

100546-84-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

100546-84-7 Usage

Chemical structure

1,8-Naphthyridine-3-carboxylic acid, 6-fluoro-1-(4-fluorophenyl)-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-, ethyl ester is a complex organic molecule with a naphthyridine core, fluorophenyl and piperazinyl substituents, and an ethyl ester group.

Core structure

The naphthyridine core is a fused ring system consisting of a pyridine and a pyrimidine ring.

Functional groups

The carboxylic acid functional group is present at the 3-position of the naphthyridine core, and the ethyl ester group is attached to the carboxylic acid.

Fluorination

The molecule contains two fluorine atoms, one on the phenyl ring and one on the naphthyridine ring, which can influence the compound's lipophilicity and metabolic stability.

Substituents

The 4-fluorophenyl and 3-methyl-1-piperazinyl substituents are attached to the naphthyridine core, potentially contributing to the compound's biological activity.

Potential pharmaceutical applications

Due to its complex structure and various functional groups, 1,8-Naphthyridine-3-carboxylic acid, 6-fluoro-1-(4-fluorophenyl)-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo- , ethyl ester may have a wide range of biological activities and could serve as a lead compound in drug discovery research.

Bioavailability

The presence of the ethyl ester group suggests that the compound may have improved bioavailability, as esters are generally more lipophilic and can more easily cross cell membranes.

Lead compound

As a result of its unique structure and potential biological activities, 1,8-Naphthyridine-3-carboxylic acid, 6-fluoro-1-(4-fluorophenyl)-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo- , ethyl ester could be a valuable starting point for the development of new drugs targeting various diseases or conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 100546-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100546-84:
(8*1)+(7*0)+(6*0)+(5*5)+(4*4)+(3*6)+(2*8)+(1*4)=87
87 % 10 = 7
So 100546-84-7 is a valid CAS Registry Number.

100546-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-fluoro-1-(4-fluorophenyl)-7-(3-methylpiperazin-1-yl)-4-oxo-1,8-naphthyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-p-fluorophenyl-6-fluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate

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:100546-84-7 SDS

100546-84-7Relevant academic research and scientific papers

Synthesis and Structure-Activity Relationships of New Arylfluoronaphthyridine Antibacterial Agents

Chu, Daniel T. W.,Fernandes, Prabhavathi B.,Claiborne, Akiyo K.,Gracey, Eugene H.,Pernet, Andre G.

, p. 2364 - 2369 (2007/10/02)

Novel arylfluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid have been prepared and their antibacterial activity evaluated.These derivatives are characterized by having a fluorine atom at 6-position, substituted amino groups at the 7-position, and substituted phenyl groups at the 1-position.The in vitro antibacterial potency is greatest when the 1-substituent is either p-fluorophenyl or o,p-difluorophenyl and the 7-substituent is a 3-amino-1-pyrrolidinyl group. 1-(2,4-Difluorophenyl)-6-fluoro-7-(3-amino-1-pyrrolidinyl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid (38) was found to possess excellent in vitro potency and in vivo efficacy.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 100546-84-7