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2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1061223-43-5 Structure
  • Basic information

    1. Product Name: 2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid
    2. Synonyms: 2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid
    3. CAS NO:1061223-43-5
    4. Molecular Formula: C9H13BFNO2
    5. Molecular Weight: 197.0144232
    6. EINECS: N/A
    7. Product Categories: Boronate Ester;Boronic Acid;Potassium Trifluoroborate
    8. Mol File: 1061223-43-5.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: 2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid(1061223-43-5)
    11. EPA Substance Registry System: 2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid(1061223-43-5)
  • 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: 1061223-43-5(Hazardous Substances Data)

1061223-43-5 Usage

Fluorophenyl group

A phenyl ring (a six-membered carbon ring with delocalized pi electrons) substituted with a fluorine atom, contributing to the compound's chemical reactivity and properties.

Dimethylaminoethyl group

A chemical group consisting of a nitrogen atom bonded to two methyl groups (CH3) and one carbon atom, which may influence the compound's reactivity and physical properties.

Organic synthesis

2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid is commonly used as a reagent in organic synthesis, particularly for Suzuki coupling reactions.

Suzuki coupling reactions

A type of carbon-carbon bond-forming reaction between an organoboron compound and an organic halide in the presence of a palladium catalyst, widely used in the construction of complex organic molecules.

Medicinal chemistry and pharmaceutical research

The compound has potential applications in these fields due to its ability to interact with biological targets, such as proteins or enzymes.

Material science and new chemical technologies

2-((diMethylaMino)Methyl)-4-fluorophenylboronic acid may have uses in these areas, potentially leading to the development of novel materials and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1061223-43-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,1,2,2 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1061223-43:
(9*1)+(8*0)+(7*6)+(6*1)+(5*2)+(4*2)+(3*3)+(2*4)+(1*3)=95
95 % 10 = 5
So 1061223-43-5 is a valid CAS Registry Number.

1061223-43-5Upstream product

1061223-43-5Downstream Products

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