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1451393-40-0

(3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid is a chemical compound characterized by the presence of a boronic acid group attached to a phenyl ring, which is substituted with a chlorine atom and a trifluoromethoxy group. This unique structure endows it with distinctive electronic and steric properties, making it a versatile reagent in various chemical reactions.

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  • 1451393-40-0 Structure

  • Basic information

    1. Product Name: (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid
    2. Synonyms: (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid
    3. CAS NO:1451393-40-0
    4. Molecular Formula: C7H5BClF3O3
    5. Molecular Weight: 240.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1451393-40-0.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: (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid(1451393-40-0)
    11. EPA Substance Registry System: (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid(1451393-40-0)

  • 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: 1451393-40-0(Hazardous Substances Data)

1451393-40-0 Usage

Uses

Used in Organic Synthesis:
(3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid is utilized as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its ability to participate in cross-coupling reactions allows for the creation of complex molecular structures with potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid is employed as a building block for the synthesis of biologically active molecules. Its unique structure and reactivity contribute to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
(3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid is also used in the agrochemical industry for the synthesis of novel compounds with pesticidal properties. Its reactivity and structural features enable the creation of new agrochemicals with improved efficacy and selectivity.
Used in Materials Science:
In the field of materials science, (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid has shown promise in the development of new functional materials. Its unique properties allow for the synthesis of materials with tailored properties, such as improved conductivity, stability, or specific interactions with other molecules.
Overall, (3-Chloro-5-(trifluoromethoxy)phenyl)boronic acid is a valuable chemical compound with diverse applications across various industries, including organic synthesis, pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactivity make it a promising building block for the development of new molecules and materials with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1451393-40-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,3,9 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1451393-40:
(9*1)+(8*4)+(7*5)+(6*1)+(5*3)+(4*9)+(3*3)+(2*4)+(1*0)=150
150 % 10 = 0
So 1451393-40-0 is a valid CAS Registry Number.

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