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1-[3-fluoro-4-(methylthio)-phenyl]ethanone is an organic compound characterized by its molecular formula C9H9FOS. It features a fluorinated phenyl ring with a methylthio group attached to the para position relative to the fluorine atom. The molecule is a derivative of acetophenone, with the ethanone group (a ketone) attached to the phenyl ring. This chemical is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, where its specific structural features may confer unique biological activities. The compound's properties, such as its reactivity and stability, are influenced by the presence of the fluorine and methylthio substituents, which can affect its electronic and steric characteristics.

2968-09-4

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2968-09-4 Usage

Chemical structure

1-[3-fluoro-4-(methylthio)-phenyl]ethanone is a chemical compound with a phenyl ring, a fluorine atom at the 3 position, a methylthio group at the 4 position, and an ethanone functional group attached to a two-carbon chain.

Functional groups

The compound contains a phenyl ring, a fluorine atom, a methylthio group, and an ethanone functional group (a ketone group attached to a two-carbon chain).

Applications

It is commonly used in organic synthesis as a building block for more complex molecules and has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and properties.

Safety

It is important to handle this chemical with care and follow safety protocols, as it may pose health risks if not handled properly.

Physical properties

The specific physical properties of 1-[3-fluoro-4-(methylthio)-phenyl]ethanone, such as melting point, boiling point, density, and solubility, are not provided in the material.

Chemical properties

The specific chemical properties of 1-[3-fluoro-4-(methylthio)-phenyl]ethanone, such as reactivity, stability, and potential reactions with other compounds, are not provided in the material.

Synthesis

The material does not provide information on the synthesis or preparation methods for 1-[3-fluoro-4-(methylthio)-phenyl]ethanone.

Purity

The material does not provide information on the purity or potential impurities of 1-[3-fluoro-4-(methylthio)-phenyl]ethanone.

Storage

The material does not provide information on the storage conditions or requirements for 1-[3-fluoro-4-(methylthio)-phenyl]ethanone.

Environmental impact

The material does not provide information on the environmental impact or potential hazards associated with 1-[3-fluoro-4-(methylthio)-phenyl]ethanone.

Check Digit Verification of cas no

The CAS Registry Mumber 2968-09-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2968-09:
(6*2)+(5*9)+(4*6)+(3*8)+(2*0)+(1*9)=114
114 % 10 = 4
So 2968-09-4 is a valid CAS Registry Number.

2968-09-4Relevant academic research and scientific papers

PYRAZOLONE DERIVATIVES AS NITROXYL DONORS

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Page/Page column 185; 237, (2016/01/29)

The disclosed subject matter provides pyrazolone derivative compounds, pharmaceutical compositions comprising such compounds, kits comprising such compounds, and methods of using such compounds or pharmaceutical compositions. In particular, the disclosed subject matter provides methods of using such compounds or pharmaceutical compositions for treating heart failure.

SULFONE DERIVATIVE

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Page/Page column 11, (2012/06/01)

Provided are a compound having an excellent hypoglycemic action, or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition having an excellent therapeutic effect and/or prophylactic effect on type 1 diabetes, type 2 diabetes, and the

Isoxazolinone antibacterial agents

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, (2008/06/13)

This invention describes isoxazolinone compounds which possess antibacterial activity and are useful in the treatment of bacterial diseases. More particularly, isoxazolinones are provided having the formula

2-Fluorobenzenesulfonyl compounds for the treatment of inflammation

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, (2008/06/13)

Methods of treating cyclooxygenase-2 mediated disorders comprising administering to a subject a therapeutically effective amount of one or more 2-fluorobenzenesulfonyl compounds corresponding to Formula I: wherein A, R1, R2, and R3 are as described in the specification, and novel 2 fluorobenzenesulfonyl compounds within Formula I.

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