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105869-37-2

Boronic acid, [2-(4-fluorophenyl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105869-37-2 Structure

  • Basic information

    1. Product Name: Boronic acid, [2-(4-fluorophenyl)ethyl]-
    2. Synonyms:
    3. CAS NO:105869-37-2
    4. Molecular Formula: C8H10BFO2
    5. Molecular Weight: 167.976
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105869-37-2.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: Boronic acid, [2-(4-fluorophenyl)ethyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boronic acid, [2-(4-fluorophenyl)ethyl]-(105869-37-2)
    11. EPA Substance Registry System: Boronic acid, [2-(4-fluorophenyl)ethyl]-(105869-37-2)

  • 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: 105869-37-2(Hazardous Substances Data)

105869-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105869-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,6 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105869-37:
(8*1)+(7*0)+(6*5)+(5*8)+(4*6)+(3*9)+(2*3)+(1*7)=142
142 % 10 = 2
So 105869-37-2 is a valid CAS Registry Number.

105869-37-2Relevant articles and documents

Visible-Light-Mediated Aerobic Oxidation of Organoboron Compounds Using in Situ Generated Hydrogen Peroxide

Weng, Wei-Zhi,Liang, Hao,Zhang, Bo

supporting information, p. 4979 - 4983 (2018/08/24)

A simple and general visible-light-mediated oxidation of organoboron compounds has been developed with rose bengal as the photocatalyst, substoichiometric Et3N as the electron donor, as well as air as the oxidant. This mild and metal-free protocol shows a broad substrate scope and provides a wide range of aliphatic alcohols and phenols in moderate to excellent yields. Notably, the robustness of this method is demonstrated on the stereospecific aerobic oxidation of organoboron compounds.

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