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1015856-57-1

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1015856-57-1 Usage

Description

6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID is a synthetic fluoroquinolone derivative with a unique chemical structure that incorporates a fluorine atom and deuterium-labeled ethyl group. 6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID exhibits potent antibacterial properties and is used in various applications across different industries.

Uses

Used in Pharmaceutical Industry:
6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID is used as an antibacterial agent for the treatment of urinary tract infections. Its unique structure allows it to target and inhibit bacterial DNA replication and protein synthesis, leading to the elimination of the infection.
Used in Research and Development:
In the field of research and development, 6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID serves as a valuable compound for studying the mechanisms of action and resistance to fluoroquinolone antibiotics. Its deuterium labeling also makes it a useful tool in mass spectrometry and other analytical techniques for tracking metabolic pathways and understanding drug metabolism.
Used in Drug Synthesis:
6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID can be utilized as a key intermediate in the synthesis of novel fluoroquinolone-based drugs with improved properties, such as enhanced antibacterial activity, reduced side effects, or increased resistance to bacterial resistance mechanisms.
Used in Veterinary Medicine:
In veterinary medicine, 6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID is used as an antibacterial agent for the treatment of various bacterial infections in animals. Its broad-spectrum activity makes it effective against a wide range of bacterial pathogens, ensuring the health and well-being of animals.
Used in Environmental Applications:
6-FLUORO-1,4-DIHYDRO-4-OXO-1-PENTADEUTEROETHYL-7-PIPERAZINO-3-QUINOLINECARBOXYLIC ACID can also be employed in environmental applications, such as water treatment and disinfection processes, to eliminate harmful bacterial contaminants and ensure the safety of water supplies.

Check Digit Verification of cas no

The CAS Registry Mumber 1015856-57-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,8,5 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1015856-57:
(9*1)+(8*0)+(7*1)+(6*5)+(5*8)+(4*5)+(3*6)+(2*5)+(1*7)=141
141 % 10 = 1
So 1015856-57-1 is a valid CAS Registry Number.

1015856-57-1 Well-known Company Product Price

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  • Sigma-Aldrich

  • (34058)  Norfloxacin-d5  VETRANAL, analytical standard

  • 1015856-57-1

  • 34058-10MG-R

  • 3,059.55CNY

  • Detail

1015856-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(<sup>2</sup>H<sub>5</sub>)Ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydro-3-quinolinecarboxylic acid

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1015856-57-1 SDS

1015856-57-1Downstream Products

1015856-57-1Relevant articles and documents

Stable isotope labeled norfloxacin and synthesis method thereof

-

, (2020/08/18)

The invention discloses stable isotope labeled norfloxacin and a synthesis method thereof. Stable isotope labeled bromoethane used as a stable isotope labeling source reacts with 6, 7-difluoro-4-hydroxyquinoline-3-carboxylic acid ethyl ester to obtain sta

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