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CAS

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1610366-45-4

pinacol 2,4,6-tribromo-3-hydroxyphenylboronate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1610366-45-4 Structure

  • Basic information

    1. Product Name: pinacol 2,4,6-tribromo-3-hydroxyphenylboronate
    2. Synonyms: pinacol 2,4,6-tribromo-3-hydroxyphenylboronate
    3. CAS NO:1610366-45-4
    4. Molecular Formula:
    5. Molecular Weight: 456.764
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1610366-45-4.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: pinacol 2,4,6-tribromo-3-hydroxyphenylboronate(CAS DataBase Reference)
    10. NIST Chemistry Reference: pinacol 2,4,6-tribromo-3-hydroxyphenylboronate(1610366-45-4)
    11. EPA Substance Registry System: pinacol 2,4,6-tribromo-3-hydroxyphenylboronate(1610366-45-4)

  • 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: 1610366-45-4(Hazardous Substances Data)

1610366-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610366-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,3,6 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1610366-45:
(9*1)+(8*6)+(7*1)+(6*0)+(5*3)+(4*6)+(3*6)+(2*4)+(1*5)=134
134 % 10 = 4
So 1610366-45-4 is a valid CAS Registry Number.

1610366-45-4Downstream Products

1610366-45-4Relevant articles and documents

Metal-free halogenation of arylboronate with N-halosuccinimide

Kamei, Toshiyuki,Ishibashi, Aoi,Shimada, Toyoshi

, p. 4245 - 4247 (2014)

Efficient bromination and chlorination of aryl pinacol boronates were accomplished without the addition of metal reagent. The reaction proceeded efficiently with electron-rich arylboronates or heteroarylboronates in DMF or acetonitrile, to afford mono-, di-, or trihalogenated aryl pinacol boronates.

Metal-free halogenation of arylboronate with N-halosuccinimide

Kamei, Toshiyuki,Ishibashi, Aoi,Shimada, Toyoshi

, p. 4245 - 4247 (2014/07/22)

Efficient bromination and chlorination of aryl pinacol boronates were accomplished without the addition of metal reagent. The reaction proceeded efficiently with electron-rich arylboronates or heteroarylboronates in DMF or acetonitrile, to afford mono-, d

Base-promoted protodeboronation of 2,6-disubstituted arylboronic acids

Lozada, Jerome,Liu, Zhibo,Perrin, David M.

, p. 5365 - 5368 (2014/06/23)

Facile based promoted deboronation of electron-deficient arylboronate esters was observed for arylboronates containing two ortho electron-withdrawing group (EWG) substituents. Among 30 representative boronates, only the diortho-substituted species underwe

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