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177942-47-1

Ethanone, 1-(3-fluoro-2-methylphenyl)(9CI) is a ketone class chemical compound characterized by the presence of a fluorine atom and a methyl group attached to a phenyl ring. It is a yellow liquid with a strong odor, known for its applications in the pharmaceutical industry as an intermediate for the synthesis of various compounds. Its unique chemical properties contribute to its value in drug discovery research and development, as well as in the production of specialty chemicals. It may also have potential applications in other industries such as agrochemicals and materials science. Due to its potential hazards, this compound should be handled with care and used in accordance with proper safety precautions.

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  • 177942-47-1 Structure

  • Basic information

    1. Product Name: Ethanone, 1-(3-fluoro-2-methylphenyl)- (9CI)
    2. Synonyms: Ethanone, 1-(3-fluoro-2-methylphenyl)- (9CI);3'-Fluoro-2'-Methylacetophenone, 97%
    3. CAS NO:177942-47-1
    4. Molecular Formula: C9H9FO
    5. Molecular Weight: 152.1655632
    6. EINECS: N/A
    7. Product Categories: HALIDE;ACETYLGROUP
    8. Mol File: 177942-47-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 210.9±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.075±0.06 g/cm3(Predicted)
    6. Refractive Index: 1.5105
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanone, 1-(3-fluoro-2-methylphenyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(3-fluoro-2-methylphenyl)- (9CI)(177942-47-1)
    11. EPA Substance Registry System: Ethanone, 1-(3-fluoro-2-methylphenyl)- (9CI)(177942-47-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 177942-47-1(Hazardous Substances Data)

177942-47-1 Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(3-fluoro-2-methylphenyl)(9CI) is used as a chemical intermediate for the synthesis of various compounds in the pharmaceutical industry. Its unique structure and chemical properties make it valuable for drug discovery research and development, contributing to the creation of new and innovative pharmaceutical products.
Used in Specialty Chemicals Production:
Ethanone, 1-(3-fluoro-2-methylphenyl)(9CI) is also utilized in the production of specialty chemicals, where its specific chemical properties are leveraged to create high-value products for various applications.
Used in Agrochemicals Industry:
Ethanone, 1-(3-fluoro-2-methylphenyl)(9CI) may have potential applications in the agrochemicals industry, where its unique structure and properties could be employed in the development of new agrochemical products.
Used in Materials Science:
Additionally, this compound may find use in materials science, where its properties could be harnessed for the development of new materials with specific characteristics and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 177942-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,4 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 177942-47:
(8*1)+(7*7)+(6*7)+(5*9)+(4*4)+(3*2)+(2*4)+(1*7)=181
181 % 10 = 1
So 177942-47-1 is a valid CAS Registry Number.

177942-47-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H32221)  3'-Fluoro-2'-methylacetophenone, 97%   

  • 177942-47-1

  • 1g

  • 604.0CNY

  • Detail

  • Alfa Aesar

  • (H32221)  3'-Fluoro-2'-methylacetophenone, 97%   

  • 177942-47-1

  • 5g

  • 2419.0CNY

  • Detail

177942-47-1Downstream Products

177942-47-1Relevant articles and documents

Lithiations directed by carboxylic acid, fluorine and chlorine: The regioselective synthesis of polysubstituted benzoic acids and acetophenones

Moyroud, Joel,Guesnet, Jean-Luc,Bennetau, Bernard,Mortier, Jacques

, p. 133 - 141 (2007/10/03)

Lithiation/electrophilic quenching of ortho-lithiated benzoates allows the totally regiocontrolled synthesis of a wide range of 2,3-, 2,3,4-, and 2,3,4,5-polysubstituted benzoic acids and related acetophenones. Elsevier,.

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