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CAS

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1565857-71-7

trimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)stannane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1565857-71-7 Structure

  • Basic information

    1. Product Name: trimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)stannane
    2. Synonyms: trimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)stannane
    3. CAS NO:1565857-71-7
    4. Molecular Formula:
    5. Molecular Weight: 366.883
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1565857-71-7.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: trimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)stannane(CAS DataBase Reference)
    10. NIST Chemistry Reference: trimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)stannane(1565857-71-7)
    11. EPA Substance Registry System: trimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)stannane(1565857-71-7)

  • 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: 1565857-71-7(Hazardous Substances Data)

1565857-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1565857-71-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,5,8,5 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1565857-71:
(9*1)+(8*5)+(7*6)+(6*5)+(5*8)+(4*5)+(3*7)+(2*7)+(1*1)=217
217 % 10 = 7
So 1565857-71-7 is a valid CAS Registry Number.

1565857-71-7Relevant articles and documents

Synthesis of trimethylstannyl arylboronate compounds by sandmeyer-type transformations and their applications in chemoselective cross-coupling reactions

Qiu, Di,Wang, Shuai,Tang, Shengbo,Meng, He,Jin, Liang,Mo, Fanyang,Zhang, Yan,Wang, Jianbo

, p. 1979 - 1988 (2014/04/03)

A synthetic method based on Sandmeyer-type reactions to access both tin- and boron-substituted arenes from nitroaniline derivatives is described. This transformation can be applied to the synthesis of a series of functionalized trimethylstannyl arylboronates. In addition, the chemoselective reaction of the Stille and Suzuki-Miyaura cross-coupling reactions is explored, and a series of m- and p-terphenyl derivatives have been synthesized by conducting consecutive one-pot Stille and Suzuki-Miyaura cross-coupling reactions.

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