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167888-38-2

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  • 3-Quinolinecarboxylicacid, 5-amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methyl-4-oxo-

    Cas No: 167888-38-2

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167888-38-2 Usage

Description

5-Amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methyl-4-oxo-3-quinolinecarboxylic acid is a complex organic compound with a unique molecular structure that features a quinoline core, a cyclopropyl group, and difluoro substitutions. 5-AMINO-1-CYCLOPROPYL-6,7-DIFLUORO-1,4-DIHYDRO-8-METHYL-4-OXO-3-QUINOLINECARBOCYLIC ACID is characterized by its potential antimicrobial properties, making it a promising candidate for the development of new antibacterial agents.

Uses

Used in Pharmaceutical Industry:
5-Amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methyl-4-oxo-3-quinolinecarboxylic acid is used as an antibacterial agent for its ability to target and inhibit the growth of various bacterial strains. Its unique structure allows it to interact with bacterial enzymes or cell components, disrupting essential processes and ultimately leading to the eradication of the bacteria.
5-AMINO-1-CYCLOPROPYL-6,7-DIFLUORO-1,4-DIHYDRO-8-METHYL-4-OXO-3-QUINOLINECARBOCYLIC ACID may be particularly useful in addressing the growing concern of antibiotic resistance, as it could offer a novel mechanism of action that differs from existing antibiotics. By incorporating this compound into new drug formulations or combining it with other antimicrobial agents, it may be possible to develop more effective treatments for bacterial infections and reduce the spread of resistant strains.

Check Digit Verification of cas no

The CAS Registry Mumber 167888-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,8,8 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 167888-38:
(8*1)+(7*6)+(6*7)+(5*8)+(4*8)+(3*8)+(2*3)+(1*8)=202
202 % 10 = 2
So 167888-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12F2N2O3/c1-5-9(15)10(16)11(17)8-12(5)18(6-2-3-6)4-7(13(8)19)14(20)21/h4,6H,2-3,17H2,1H3,(H,20,21)

167888-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-1-cyclopropyl-6,7-difluoro-8-methyl-4-oxoquinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Quinolinecarboxylicacid,5-amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methyl-4-oxo

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:167888-38-2 SDS

167888-38-2Downstream Products

167888-38-2Relevant articles and documents

Substituted aminocycloalkylpyrrolidine derivatives and cis-substituted aminocycloalkylpyrrolidine derivatives

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, (2008/06/13)

An antimicrobial drug having excellent antimicrobial activity and high safety is disclosed, which comprises as an active ingredient, a quinolone-derivative having a substituted aminocycloalkylpyrrolidine as a substituent and which is further substituted w

5-amino-8-methyl-7-pyrrolidinylquinoline-3-carboxylic acid derivative

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, (2008/06/13)

A 5-amino-8-methyl-7-pyrrolidinylquinoline-3-carboxylic acid derivative represented by the general formula: STR1 wherein R1 is a hydrogen atom or a lower alkyl group; R2 is a hydrogen atom, a lower alkyl group, a lower alkanoyl group, a halogenated lower alkanoyl group or a residue of carboxylic acid ester; R3 is a hydrogen atom or a lower alkyl group; R4, R5 or R6 are each independently a hydrogen atom or a lower alkyl group; or two of R4, R5 and R6 may be taken together to form a --(CH2)n -group wherein n is 1 or 2, a stereoisomer thereof, or a pharmacologically acceptable salt thereof, the process for preparing these compounds, a pharmaceutical composition comprising an effective amount of these compounds and methods for the treatment of infectious diseases through the administration to patients of an effective amount of these compounds, and intermediates of these compounds are disclosed. These compounds are effective as antibacterial agents.

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