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2-OXAZOLIDINONE, 5-(AZIDOMETHYL)-3-(3-FLUOROPHENYL)-, (5R)is a unique oxazolidinone derivative characterized by its 5R stereochemistry and a distinctive chemical structure that features an oxazolidinone ring, an azidomethyl group, and a 3-fluorophenyl moiety. 2-OXAZOLIDINONE, 5-(AZIDOMETHYL)-3-(3-FLUOROPHENYL)-, (5R)holds promise in the realm of medicinal chemistry and pharmaceuticals due to its distinctive structural attributes and potential biological activities, which warrant further research and exploration to uncover its full spectrum of applications.

149524-44-7

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149524-44-7 Usage

Uses

Used in Medicinal Chemistry:
2-OXAZOLIDINONE, 5-(AZIDOMETHYL)-3-(3-FLUOROPHENYL)-, (5R)is used as a compound of interest in medicinal chemistry for its potential to contribute to the development of novel therapeutic agents. Its unique structure may offer new avenues for drug design, particularly in targeting specific biological pathways or receptors.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-OXAZOLIDINONE, 5-(AZIDOMETHYL)-3-(3-FLUOROPHENYL)-, (5R)is utilized as a key intermediate or building block in the synthesis of new pharmaceuticals. Its incorporation into drug molecules could enhance their efficacy, selectivity, or pharmacokinetic properties, leading to improved treatments for various diseases and conditions.
Used in Research and Development:
2-OXAZOLIDINONE, 5-(AZIDOMETHYL)-3-(3-FLUOROPHENYL)-, (5R)serves as a valuable research tool in academic and industrial laboratories. It is used to investigate the structure-activity relationships of oxazolidinone derivatives and to explore their potential as bioactive molecules, which can lead to the discovery of new drugs or drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 149524-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,5,2 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149524-44:
(8*1)+(7*4)+(6*9)+(5*5)+(4*2)+(3*4)+(2*4)+(1*4)=147
147 % 10 = 7
So 149524-44-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9FN4O2/c11-7-2-1-3-8(4-7)15-6-9(5-13-14-12)17-10(15)16/h1-4,9H,5-6H2/t9-/m0/s1

149524-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(azidomethyl)-3-(3-fluorophenyl)-1,3-oxazolidin-2-one

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 -
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More Details:149524-44-7 SDS

149524-44-7Relevant academic research and scientific papers

Synthesis and in vitro activity of novel 1,2,4-triazolo[4,3-a]pyrimidine oxazolidinone antibacterial agents. Part II

Khera, Manoj Kumar,Cliffe, Ian A.,Prakash, Om

, p. 5266 - 5269 (2011/10/02)

The synthesis and antibacterial activity of 1,2,4-triazolo[4,3-a]pyrimidine oxazolidinones is reported. Compound 3e with a 2,4-disubstituted thiophene ring was found to be a potent inhibitor of Gram-positive pathogens and was 4-16-fold more potent than Linezolid.

BIFUNCTIONAL MACROLIDE HETEROCYCLIC COMPOUNDS AND MEHTODS OF MAKING AND USING THE SAME

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Page/Page column 62, (2010/02/11)

The present invention relates generally to the field of anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents. More particularly, the invention relates to a family of bifunctional compounds useful as therapeutic agents. These com

Substituted aryl- and heteroaryl-phenyloxazolidinones

-

, (2008/06/13)

The present invention discloses novel substituted aryl- and heteroarylphenyloxazolidinones which are useful as anti-bacterial agents. More specifically, the substituted aryl- and heteroarylphenyloxazolidinones of the invention are characterized by oxazoli

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