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F5C6CH2B(pinacolato) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1075719-80-0 Structure
  • Basic information

    1. Product Name: F5C6CH2B(pinacolato)
    2. Synonyms: F5C6CH2B(pinacolato)
    3. CAS NO:1075719-80-0
    4. Molecular Formula:
    5. Molecular Weight: 308.056
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1075719-80-0.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: F5C6CH2B(pinacolato)(CAS DataBase Reference)
    10. NIST Chemistry Reference: F5C6CH2B(pinacolato)(1075719-80-0)
    11. EPA Substance Registry System: F5C6CH2B(pinacolato)(1075719-80-0)
  • 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: 1075719-80-0(Hazardous Substances Data)

1075719-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1075719-80-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,5,7,1 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1075719-80:
(9*1)+(8*0)+(7*7)+(6*5)+(5*7)+(4*1)+(3*9)+(2*8)+(1*0)=170
170 % 10 = 0
So 1075719-80-0 is a valid CAS Registry Number.

1075719-80-0Downstream Products

1075719-80-0Relevant articles and documents

Iridium-catalyzed preparation of silylboranes by silane borylation and their use in the catalytic borylation of arenes

Boebel, Timothy A.,Hartwig, John F.

, p. 6013 - 6019 (2008)

Silylboranes are versatile reagents for transition metal-catalyzed reactions of unsaturated organic molecules. These reagents are typically prepared by the addition of a silyl lithium species to a boron electrophile. However, the need to generate anionic silane reagents limits the scope of silylboranes that can be readily obtained. Here, we describe the synthesis of trialkylsilylboranes by the borylation of silanes catalyzed by iridium complexes. The reaction of trialkylhydrosilanes with B2pin 2 catalyzed by the combination of [Ir(OMe)cod]2 and 4,4′-di-tert-butylbipyridine forms trialkylsilylboronic esters. In addition, we show that these trialkylsilylboranes serve as boron sources for the iridium-catalyzed borylation of aryl C-H bonds. In contrast to diboron reagents, the silylboranes react with methylarenes at both the aryl and methyl C-H bonds.

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