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4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile is a chemical compound with the molecular formula C14H7F2NO. It is a nitrile derivative of benzenecarbonitrile, featuring two fluorine atoms and a phenylcarbonyl group attached to the benzene ring. 4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile is known for its versatile chemical properties and reactivity, making it a valuable building block in the synthesis of various organic compounds.

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  • 395100-11-5 Structure
  • Basic information

    1. Product Name: 4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile
    2. Synonyms: 4-Fluoro-3-(4-fluorobenzoyl)benzonitrile;4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile
    3. CAS NO:395100-11-5
    4. Molecular Formula: C14H7F2NO
    5. Molecular Weight: 243.2082864
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 395100-11-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.32
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile(395100-11-5)
    11. EPA Substance Registry System: 4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile(395100-11-5)
  • 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: 395100-11-5(Hazardous Substances Data)

395100-11-5 Usage

Uses

Used in Pharmaceutical Industry:
4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile is utilized as an intermediate in the synthesis of a wide range of drugs and pharmaceuticals. Its unique structure and functional groups contribute to the development of new and innovative medications.
Used in Organic Synthesis:
As a reagent in organic synthesis, 4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile plays a crucial role in the preparation of various organic compounds. Its presence of the nitrile group enhances its reactivity and makes it a key component in the synthesis process.
Used in Chemical Research:
4-Fluoro-3-[(4-fluorophenyl)carbonyl]benzenecarbonitrile is also employed in chemical research to study and understand the properties and reactions of similar compounds. Its unique structure and reactivity provide valuable insights into the development of new chemical processes and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 395100-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,1,0 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 395100-11:
(8*3)+(7*9)+(6*5)+(5*1)+(4*0)+(3*0)+(2*1)+(1*1)=125
125 % 10 = 5
So 395100-11-5 is a valid CAS Registry Number.

395100-11-5Upstream product

395100-11-5Downstream Products

395100-11-5Relevant articles and documents

Indazole compounds, compositions thereof and methods of treatment therewith

-

, (2008/06/13)

This invention is generally directed to the use of Indazole Compounds for treating or preventing diseases associated with protein kinases, including tyrosine kinases, such as proliferative diseases, inflammatory diseases, abnormal angiogenesis and diseases related thereto, atherosclerosis, macular degeneration, diabetes, obesity, pain and others. The methods comprise the administration to a patient in need thereof of an effective amount of an indazole compound that inhibits, modulates or regulates tyrosine kinase signal transduction. Novel indazole compounds or pharmaceutically acceptable salt thereof are presented herein.

Methods for treating an inflammatory condition or inhibiting JNK

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, (2008/06/13)

This invention is generally directed to Indazole Derivatives having the following structure: 1 or pharmaceutically acceptable salt thereof, wherein R1, R2 and A are as defined herein. Such compounds have utility in the treatment of a wide range of diseases and disorders that are responsive to JNK inhibition, such as an inflammatory disease or disorder. Thus, methods of treating such diseases and disorders are also disclosed, as are pharmaceutical compositions containing one or more compounds of the above compounds.

Indazole derivatives as JNK inhibitors and compositions and methods related thereto

-

, (2008/06/13)

Compounds having activity as selective inhibitors of JNK are disclosed. The compounds of this invention are indazole derivatives having the following structure: wherein R1, R2 and A are as defined herein. Such compounds have utility in the treatment of a wide range of conditions that are responsive to JNK inhibition. Thus, methods of treating such conditions are also disclosed, as are pharmaceutical compositions containing one or more compounds of the above compounds.

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