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CAS

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1067228-89-0

(2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid is a boronic acid derivative with the molecular formula C8H7BF6O3. It is a white crystalline powder that is insoluble in water but soluble in organic solvents. (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid is often used in organic synthesis and pharmaceutical research due to its unique structure and properties.

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  • 1067228-89-0 Structure

  • Basic information

    1. Product Name: (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid
    2. Synonyms: (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid
    3. CAS NO:1067228-89-0
    4. Molecular Formula:
    5. Molecular Weight: 287.954
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1067228-89-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid(1067228-89-0)
    11. EPA Substance Registry System: (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid(1067228-89-0)

  • 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: 1067228-89-0(Hazardous Substances Data)

1067228-89-0 Usage

Uses

Used in Organic Synthesis:
(2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid is used as a reagent in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds. Its trifluoromethyl groups on the phenyl ring make it a useful electron-withdrawing group, enhancing the reactivity and selectivity of certain chemical reactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid is used as a building block for the synthesis of various drug candidates. Its unique structure and properties make it a valuable tool for the development of new medications.
Used in the Formation of Arylboronic Esters:
(2-methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid is also used in the formation of arylboronic esters, which are important intermediates in organic chemistry and have applications in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1067228-89-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,2,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1067228-89:
(9*1)+(8*0)+(7*6)+(6*7)+(5*2)+(4*2)+(3*8)+(2*8)+(1*9)=160
160 % 10 = 0
So 1067228-89-0 is a valid CAS Registry Number.

1067228-89-0Upstream product

1067228-89-0Downstream Products

1067228-89-0Relevant articles and documents

2-Arylpyrimidines: Novel CRF-1 receptor antagonists

Yoon, Taeyoung,De Lombaert, Stephane,Brodbeck, Robbin,Gulianello, Michael,Krause, James E.,Hutchison, Alan,Horvath, Raymond F.,Ge, Ping,Kehne, John,Hoffman, Diane,Chandrasekhar, Jayaraman,Doller, Dario,Hodgetts, Kevin J.

scheme or table, p. 4486 - 4490 (2009/04/08)

The design, synthesis and structure-activity relationship studies of a novel series of CRF-1 receptor antagonists, the 2-arylpyrimidines, are described. The effects of substitution on the aromatic ring and the pyrimidine core on CRF-1 receptor binding wer

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