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1704069-57-7

(3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is a boronic acid derivative with the molecular formula C14H14BNO4. It is a chemical compound that features a boron atom bonded to a carbaMoylphenyl group and a methoxyphenyl group. This unique structure makes it a valuable tool in organic synthesis and medicinal chemistry for constructing carbon-carbon and carbon-heteroatom bonds.

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  • 1704069-57-7 Structure

  • Basic information

    1. Product Name: (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid
    2. Synonyms: (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid
    3. CAS NO:1704069-57-7
    4. Molecular Formula: C14H14BNO4
    5. Molecular Weight: 271.07626
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1704069-57-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.28±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 7.80±0.10(Predicted)
    10. CAS DataBase Reference: (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid(1704069-57-7)
    12. EPA Substance Registry System: (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid(1704069-57-7)

  • 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: 1704069-57-7(Hazardous Substances Data)

1704069-57-7 Usage

Uses

Used in Organic Synthesis:
(3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is used as a synthetic intermediate for the creation of various organic compounds. Its ability to form reversible covalent bonds with diols and other nucleophiles makes it a versatile building block in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is used as a key component in the development of pharmaceutical compounds. Its unique structure allows for the formation of new bonds that can contribute to the creation of novel drug candidates with potential therapeutic applications.
Used in Drug Development:
(3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is utilized in drug development as a building block for the synthesis of pharmaceutical compounds. Its properties enable the design and synthesis of new molecules with potential medicinal properties, contributing to the advancement of new treatments and therapies.
Used in Chemical Biology:
In chemical biology, (3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is used for its ability to form reversible covalent bonds with biological molecules, such as diols. This feature makes it an important tool in the study of biological systems and the development of bioactive compounds.
Used in Materials Science:
(3-((3-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is also used in materials science for the development of new materials with unique properties. Its ability to form reversible covalent bonds can be harnessed to create materials with specific characteristics, such as self-healing or adaptive properties, for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1704069-57-7 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 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1704069-57:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*9)+(2*5)+(1*7)=157
157 % 10 = 7
So 1704069-57-7 is a valid CAS Registry Number.

1704069-57-7Upstream product

1704069-57-7Downstream Products

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