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863248-36-6

2-FLUORO-5-PROPOXYPHENYLBORONIC ACID is a boronic acid derivative with the molecular formula C9H12BFO3. It features a phenyl ring with a fluorine atom and a propoxy group attached, providing unique electronic and steric properties. This chemical compound is widely utilized in organic synthesis and medicinal chemistry for the preparation of pharmaceutical compounds and organic materials.

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  • 863248-36-6 Structure

  • Basic information

    1. Product Name: 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID
    2. Synonyms: 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID
    3. CAS NO:863248-36-6
    4. Molecular Formula: C9H12BFO3
    5. Molecular Weight: 198
    6. EINECS: N/A
    7. Product Categories: Aryl;Boronic Acids;Boronic Acids and Derivatives
    8. Mol File: 863248-36-6.mol

  • Chemical Properties

    1. Melting Point: 82-87 °C(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID(863248-36-6)
    11. EPA Substance Registry System: 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID(863248-36-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 863248-36-6(Hazardous Substances Data)

863248-36-6 Usage

Uses

Used in Organic Synthesis:
2-FLUORO-5-PROPOXYPHENYLBORONIC ACID is used as a reagent in organic synthesis for its versatile reactivity due to the boronic acid functional group. It is particularly valuable in the synthesis of biaryl compounds, which are important structural motifs in various organic materials and pharmaceuticals.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID is used as a key intermediate in the preparation of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved properties, such as enhanced potency, selectivity, and bioavailability.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
2-FLUORO-5-PROPOXYPHENYLBORONIC ACID is employed as a coupling partner in Suzuki-Miyaura cross-coupling reactions, a widely used method for the formation of carbon-carbon bonds in organic synthesis. This reaction allows for the efficient construction of complex molecular architectures, facilitating the synthesis of diverse organic compounds and pharmaceuticals.
Used in Chemical Research and Development:
In the field of chemical research and development, 2-FLUORO-5-PROPOXYPHENYLBORONIC ACID is utilized for exploring new reaction pathways and developing innovative synthetic methods. Its unique electronic and steric properties make it a valuable tool for studying the reactivity and selectivity of various chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 863248-36-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,2,4 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 863248-36:
(8*8)+(7*6)+(6*3)+(5*2)+(4*4)+(3*8)+(2*3)+(1*6)=186
186 % 10 = 6
So 863248-36-6 is a valid CAS Registry Number.

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