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(10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid, also known as ABAB boronic acid, is an organic compound that features a boronic acid group attached to a biphenyl and anthracene moiety. This unique structure endows it with distinctive reactivity and makes it a valuable building block in the synthesis of complex organic molecules, particularly for applications in pharmaceuticals, agrochemicals, and materials science.

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  • 400607-48-9 Structure
  • Basic information

    1. Product Name: (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid
    2. Synonyms: (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid
    3. CAS NO:400607-48-9
    4. Molecular Formula: C26H19BO2
    5. Molecular Weight: 374.23886
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 400607-48-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    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: (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid(400607-48-9)
    11. EPA Substance Registry System: (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid(400607-48-9)
  • 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: 400607-48-9(Hazardous Substances Data)

400607-48-9 Usage

Uses

Used in Organic Synthesis:
(10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid is used as a reagent in organic synthesis for the creation of various functionalized materials. Its boronic acid group allows for the formation of carbon-carbon bonds, which is crucial in constructing complex molecular structures.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic chemistry, (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid is utilized as a key component in Suzuki-Miyaura cross-coupling reactions. It serves as a nucleophile to form carbon-carbon bonds with electrophiles, facilitating the synthesis of a wide range of organic compounds.
Used in Pharmaceutical Industry:
(10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid is used as a building block in the pharmaceutical industry for the development of new drugs. Its unique structure allows for the creation of molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid is employed as a precursor in the synthesis of agrochemicals. Its reactivity and structural features contribute to the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Materials Science:
(10-[1,1'-Biphenyl]-2-yl-9-anthracenyl)boronic acid is used as a component in the synthesis of advanced materials in materials science. Its incorporation into materials can lead to the development of new properties, such as improved conductivity, stability, or specific interactions with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 400607-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,6,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 400607-48:
(8*4)+(7*0)+(6*0)+(5*6)+(4*0)+(3*7)+(2*4)+(1*8)=99
99 % 10 = 9
So 400607-48-9 is a valid CAS Registry Number.

400607-48-9Downstream Products

400607-48-9Relevant articles and documents

Naphthyl benzofuran and anthracene derivative, preparation method and application thereof and device

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Paragraph 0050, (2018/07/10)

The invention belongs to the field of application sciences of organic photoelectric materials and specifically relates to a naphthyl benzofuran and anthracene derivative, a preparation method and application thereof and a device. The naphthyl benzofuran a

ASYMMETRIC MONOANTHRACENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE UTILIZING THE SAME

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Page/Page column 35, (2008/06/13)

Provided are an asymmetric monoanthracene derivative having a specific structure, a material for an organic EL device comprising the above asymmetric monoanthracene derivative and an organic EL device in which an organic thin film layer comprising a single layer or plural layers including a luminescent layer is interposed between a cathode and an anode, wherein at least one of the above organic thin film layers contains the asymmetric monoanthracene derivative described above in the form of a single component or a mixed component. Provided are an organic electroluminescent (EL) device having a high luminous efficiency and a long life, an asymmetric monoanthracene derivative which materializes the same and a material for an organic EL device.

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