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1246027-13-3

4-dimesitylboron-4'-mesitylbiphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1246027-13-3 Structure

  • Basic information

    1. Product Name: 4-dimesitylboron-4'-mesitylbiphenyl
    2. Synonyms:
    3. CAS NO:1246027-13-3
    4. Molecular Formula:
    5. Molecular Weight: 520.566
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1246027-13-3.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: 4-dimesitylboron-4'-mesitylbiphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-dimesitylboron-4'-mesitylbiphenyl(1246027-13-3)
    11. EPA Substance Registry System: 4-dimesitylboron-4'-mesitylbiphenyl(1246027-13-3)

  • 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: 1246027-13-3(Hazardous Substances Data)

1246027-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1246027-13-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,0,2 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1246027-13:
(9*1)+(8*2)+(7*4)+(6*6)+(5*0)+(4*2)+(3*7)+(2*1)+(1*3)=123
123 % 10 = 3
So 1246027-13-3 is a valid CAS Registry Number.

1246027-13-3Upstream product

1246027-13-3Downstream Products

1246027-13-3Relevant articles and documents

Reactivity of aryldimesitylboranes under suzuki-miyaura coupling conditions

Wang, Nan,Hudson, Zachary M.,Wang, Suning

experimental part, p. 4007 - 4011 (2011/01/03)

Sterically protected triarylboron compounds such as BMes2(Ar) have important applications in organic optoelectronic devices and chemical sensors. Furthermore, the Suzuki-Miyaura cross-coupling reaction is the most commonly used method for building the π skeletons of such conjugated materials. We have found that BMes2(Ar) can also be a highly active and effective coupling partner under typical Suzuki-Miyaura coupling conditions. For BMes2(p-Br-Ph), self-coupling leads to the formation of oligomers Mes2B-(Ph)n-Mes, where the products with n = 1 (1), 2 (2), 3 (3), 4 (4) have been isolated and fully characterized. Examination of cross-coupling reactions of BMes2(Ph) with various aryl bromides has established the generality of BMes2(Ar) as a coupling partner.

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