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1704067-48-0

(3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid is a boronic acid derivative characterized by a phenyl ring with two fluorine atoms at the 3 and 4 positions, and a pyrrolidinyl group attached at the 5 position. (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid is known for its ability to form stable complexes with diols, amines, and other Lewis bases, which makes it a versatile building block in organic synthesis and medicinal chemistry for the preparation of pharmaceuticals and other biologically active molecules.

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  • 1704067-48-0 Structure

  • Basic information

    1. Product Name: (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid
    2. Synonyms: (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid
    3. CAS NO:1704067-48-0
    4. Molecular Formula: C10H12BF2NO2
    5. Molecular Weight: 227.0155864
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1704067-48-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 403.8±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.33±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 7.60±0.11(Predicted)
    10. CAS DataBase Reference: (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid(1704067-48-0)
    12. EPA Substance Registry System: (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid(1704067-48-0)

  • 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: 1704067-48-0(Hazardous Substances Data)

1704067-48-0 Usage

Uses

Used in Organic Synthesis:
(3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid is used as a building block for the synthesis of complex organic molecules, leveraging its ability to form stable complexes with various Lewis bases.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid is used as a key component in the development of pharmaceuticals, due to its potential to participate in hydrogen bonding and other interactions in biological systems.
Used in Suzuki-Miyaura Coupling:
(3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid is utilized as a reactant in Suzuki-Miyaura coupling reactions, a widely used method for forming carbon-carbon bonds, which is crucial for the synthesis of various organic compounds and pharmaceuticals.
Used in Drug Discovery and Development:
(3,4-difluoro-5-(pyrrolidin-1-yl)phenyl)boronic acid is of interest in drug discovery and development due to the pyrrolidinyl group's potential to engage in hydrogen bonding and other interactions that can be beneficial for the design of new drugs with improved pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1704067-48-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1704067-48:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*7)+(2*4)+(1*8)=150
150 % 10 = 0
So 1704067-48-0 is a valid CAS Registry Number.

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