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1-(4-Amino-2-fluorophenyl)ethanone is a chemical compound that belongs to the class of organic compounds known as benzene and substituted derivatives. It is characterized by an aromatic hexagonal carbon ring with a ketone (ethanone) group attached to the carbon, along with an amino (NH2) and a fluorine atom on the phenyl ring. 1-(4-AMINO-2-FLUOROPHENYL)ETHANONE is primarily used and handled in a laboratory setting, and its specific potential applications or toxicity are not well-known, necessitating further research.

112279-56-8

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112279-56-8 Usage

Uses

1-(4-Amino-2-fluorophenyl)ethanone is used as a chemical intermediate in various scientific and industrial applications. The exact uses are not explicitly mentioned in the provided materials, but its presence in the class of benzene and substituted derivatives suggests that it may be involved in the synthesis of other compounds or used in research and development processes.
Used in Chemical Research and Development:
1-(4-Amino-2-fluorophenyl)ethanone is used as a chemical intermediate for the synthesis of other compounds, contributing to the advancement of chemical research and development.
Used in Laboratory Settings:
1-(4-Amino-2-fluorophenyl)ethanone is used in laboratory settings for various scientific experiments and analyses, given its unique chemical structure and properties. Its application in this context is primarily for research purposes, as its potential toxicity and specific uses are not well-understood at this time.

Check Digit Verification of cas no

The CAS Registry Mumber 112279-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,7 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112279-56:
(8*1)+(7*1)+(6*2)+(5*2)+(4*7)+(3*9)+(2*5)+(1*6)=108
108 % 10 = 8
So 112279-56-8 is a valid CAS Registry Number.

112279-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-AMINO-2-FLUOROPHENYL)ETHANONE

1.2 Other means of identification

Product number -
Other names 4'-AMINO-2'-FLUOROACETOPHENONE

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:112279-56-8 SDS

112279-56-8Downstream Products

112279-56-8Relevant academic research and scientific papers

Positron Emission Tomography Imaging of Staphylococcus aureus Infection Using a Nitro-Prodrug Analogue of 2-[18F]F- p-Aminobenzoic Acid

Daryaee, Fereidoon,Li, Yong,Meimetis, Labros,Noh, Doyoung,Si, Yuanyuan,Smith-Jones, Peter M.,Tonge, Peter J.,Turkman, Nashaat,Walker, Stephen G.,Yoon, Grace E.

, p. 2249 - 2259 (2020)

Deep-seated bacterial infections caused by pathogens such as Staphylococcus aureus are difficult to diagnose and treat and are thus a major threat to human health. In previous work we demonstrated that positron emission tomography (PET) imaging with 2-[18

POSITRON IMAGING TOMOGRAPHY IMAGING AGENT COMPOSITION AND METHOD FOR DETECTION OF BACTERIAL INFECTION

-

Page/Page column 42, (2021/11/13)

This invention provides a composition comprising the compound having the structure: ethyl 2-[19F]F-4-nitrobenzoate, and at least one acceptable carrier. This invention also provides a method of detecting the presence of or location of bacteria

Preparation method of 4-chloro-2-fluoro-5-nitroacetophenone

-

Paragraph 0026-0029, (2020/01/25)

The invention discloses a preparation method of 4-chloro-2-fluoro-5-nitroacetophenone, the preparation method is characterized in that m-fluoroaniline is taken as an initial raw material, and the 4-chloro-2-fluoro-5-nitroacetophenone is obtained through acetylation amino protection, Friedel-Crafts acylation reaction, hydrolysis reaction, Sandmeyer reaction and final nitration, and the preparationmethod has the advantages of easily available raw materials, low reaction condition requirement, few side reactions and high yield.

P -Toluenesulfonic Acid Induced Conversion of Fluorinated Trimethylsilylethynylanilines into Aminoacetophenones: Versatile Precursors for the Synthesis of Benzoazaheterocycles

Politanskaya, Larisa,Tretyakov, Evgeny

, p. 555 - 564 (2017/11/03)

A simple and efficient approach to the synthesis of fluorinated amino-substituted acetophenones in good to excellent yields is reported. The heart of the proposed method consists of conversion of a Me 3 Si-C≡C- moiety into a MeC(=O)- group in the presence of p -tolu ene sulfonic acid (p -TSA) passing a stage of ethynylaniline formation. The reaction is metal-free, proceeds under mild conditions, and uses readily available starting compounds (trimethylsilylarylacetylene derivatives). The reaction provides access to amino-substituted acetophenones, which may serve as precursors for the synthesis of polyfluorinated azaheterocycles, having potential anticarcinogenic activity.

Anthranilonitrile derivatives as useful agents for promoting growth, improving feed efficiency, and for increasing the lean meat to fat ratio of warm-blooded animals

-

, (2008/06/13)

There are provided novel anthranilonitrile derivatives and related compounds which are useful for promoting growth, improving feed efficiency and for increasing the lean meat to fat ratio of warm-blooded animals.

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