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5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE is a chemical compound that belongs to the class of imidazole derivatives. It is characterized by the presence of a 4-fluorophenyl group attached to the imidazole ring. 5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE has potential applications in medicinal chemistry and drug development due to its potential to exhibit biological activity in various biological pathways. Its unique structure and properties make it a valuable target for pharmacological research, and it may be used as a building block in the synthesis of novel pharmaceuticals. Additionally, it may also have potential industrial applications in various chemical processes and reactions. Overall, 5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE has the potential to be utilized in various fields, including pharmaceuticals, biotechnology, and chemical industries.

60472-17-5

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60472-17-5 Usage

Uses

Used in Pharmaceutical Industry:
5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and potential biological activity make it a promising candidate for the synthesis of novel pharmaceuticals targeting various diseases and conditions.
Used in Medicinal Chemistry Research:
5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE is used as a research compound in medicinal chemistry to study its potential biological activity and interactions with biological targets. This research can lead to the discovery of new drug candidates and a better understanding of the underlying mechanisms of various diseases.
Used in Chemical Industry:
5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE is used as a building block or reagent in various chemical processes and reactions. Its unique structure and properties can contribute to the development of new chemical products and materials with specific applications in different industries.
Used in Biotechnology:
5-(4-FLUOROPHENYL)-1H-IMIDAZOL-2-AMINE may have potential applications in biotechnology, such as in the development of new biosensors, diagnostic tools, or as a component in biocatalytic processes. Its unique structure and potential interactions with biological systems make it a valuable compound for exploration in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 60472-17-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,7 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60472-17:
(7*6)+(6*0)+(5*4)+(4*7)+(3*2)+(2*1)+(1*7)=105
105 % 10 = 5
So 60472-17-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8FN3/c10-7-3-1-6(2-4-7)8-5-12-9(11)13-8/h1-5H,(H3,11,12,13)

60472-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-fluorophenyl)-1H-iMidazol-2-aMine

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:60472-17-5 SDS

60472-17-5Downstream Products

60472-17-5Relevant academic research and scientific papers

Structure-activity relationship of 4(5)-aryl-2-amino-1 H -imidazoles, N 1-substituted 2-aminoimidazoles and imidazo[1,2- a ]pyrimidinium salts as inhibitors of biofilm formation by salmonella typhimurium and pseudomonas aeruginosa

Steenackers, Hans P. L.,Ermolatev, Denis S.,Savaliya, Bharat,De Weerdt, Ami,De Coster, David,Shah, Anamik,Van Der Eycken, Erik V.,De Vos, Dirk E.,Vanderleyden, Jozef,De Keersmaecker, Sigrid C. J.

, p. 472 - 484 (2011/04/15)

A library of 112 4(5)-aryl-2-amino-1H-imidazoles, 4,5-diphenyl-2-amino-1H- imidazoles, and N1-substituted 4(5)-phenyl-2-aminoimidazoles was synthesized and tested for the antagonistic effect against biofilm formation by Salmonella Typhimurium and Pseudomo

COMPOUNDS, COMPOSITIONS AND METHODS FOR CONTROLLING BIOFILMS

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Page/Page column 29, (2011/07/30)

This invention relates to substituted 2-aminoimidazoles and their imidazo[1,2- a]pyrimidinium salts precursors being active against biofilm formation. The present invention also relates to antimicrobial compositions comprising a microbial biofilm formatio

Microwave-assisted synthesis of substituted 2-amino-1H-imidazoles from imidazo[1,2-a]pyrimidines

Ermolat'ev,Svidritsky,Babaev,Van der Eycken

supporting information; experimental part, p. 5218 - 5220 (2009/12/06)

An efficient method for the synthesis of mono- and disubstituted 2-amino-1H-imidazoles via microwave-assisted hydrazinolysis of substituted imidazo[1,2-a]pyrimidines is reported. This protocol avoids strong acidic conditions and is superior to the classic

Method for inhibiting advanced glycosylation of proteins using aminosubstituted imidazoles

-

, (2008/06/13)

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging), Accordingly, a composition is disclosed which comprises 2-aminoimidazoles capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation, The method comprises contacting the target protein with the composition, Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.

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