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1-(2-Amino-4,6-difluorophenyl)ethanone is a chemical compound with the molecular formula C8H7F2NO. It is classified as an ethanone, which is a type of ketone molecule, and contains an amino group and two fluorine atoms attached to a phenyl ring. 1-(2-AMino-4,6-difluorophenyl)ethanone may have potential applications in pharmaceutical research and drug development due to its structural features. Its properties and reactivity make it a potentially valuable building block for the synthesis of other organic compounds with specific functional groups or biological activities.

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  • 1632285-92-7 Structure
  • Basic information

    1. Product Name: 1-(2-AMino-4,6-difluorophenyl)ethanone
    2. Synonyms: 1-(2-AMino-4,6-difluorophenyl)ethanone
    3. CAS NO:1632285-92-7
    4. Molecular Formula: C8H7F2NO
    5. Molecular Weight: 171.1440864
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1632285-92-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 264.8±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.299±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    8. Solubility: N/A
    9. PKA: 0.28±0.10(Predicted)
    10. CAS DataBase Reference: 1-(2-AMino-4,6-difluorophenyl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(2-AMino-4,6-difluorophenyl)ethanone(1632285-92-7)
    12. EPA Substance Registry System: 1-(2-AMino-4,6-difluorophenyl)ethanone(1632285-92-7)
  • 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: 1632285-92-7(Hazardous Substances Data)

1632285-92-7 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
1-(2-Amino-4,6-difluorophenyl)ethanone is used as a building block for the synthesis of other organic compounds with specific functional groups or biological activities. Its unique structure, which includes an amino group and two fluorine atoms attached to a phenyl ring, makes it a promising candidate for the development of new pharmaceuticals and drugs.
Used in Organic Synthesis:
1-(2-Amino-4,6-difluorophenyl)ethanone is used as a key intermediate in the synthesis of various organic compounds. Its reactivity and structural features allow for the creation of a wide range of molecules with different functional groups, making it a valuable asset in the field of organic chemistry.
Used in Chemical Research:
1-(2-Amino-4,6-difluorophenyl)ethanone is used as a research tool to study the properties and reactivity of similar compounds. Understanding the behavior of this molecule can provide insights into the development of new synthetic methods and the design of novel chemical structures.
Used in the Development of Fluorinated Compounds:
1-(2-Amino-4,6-difluorophenyl)ethanone is used in the development of fluorinated compounds, which are known for their unique properties and applications in various fields, including pharmaceuticals, agrochemicals, and materials science. The presence of two fluorine atoms in the molecule makes it an interesting starting point for the synthesis of fluorinated derivatives with potential applications in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 1632285-92-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,3,2,2,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1632285-92:
(9*1)+(8*6)+(7*3)+(6*2)+(5*2)+(4*8)+(3*5)+(2*9)+(1*2)=167
167 % 10 = 7
So 1632285-92-7 is a valid CAS Registry Number.

1632285-92-7Downstream Products

1632285-92-7Relevant articles and documents

DNA-PK INHIBITORS

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Paragraph 00467, (2019/08/08)

The present invention relates to compounds useful as inhibitors of DNA-PK. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various diseases, conditions, or disorders.

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