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1,1-dibromo-2,3,4,5-tetraphenylstannole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55690-98-7 Structure
  • Basic information

    1. Product Name: 1,1-dibromo-2,3,4,5-tetraphenylstannole
    2. Synonyms: 1,1-dibromo-2,3,4,5-tetraphenylstannole
    3. CAS NO:55690-98-7
    4. Molecular Formula:
    5. Molecular Weight: 634.985
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55690-98-7.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: 1,1-dibromo-2,3,4,5-tetraphenylstannole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-dibromo-2,3,4,5-tetraphenylstannole(55690-98-7)
    11. EPA Substance Registry System: 1,1-dibromo-2,3,4,5-tetraphenylstannole(55690-98-7)
  • 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: 55690-98-7(Hazardous Substances Data)

55690-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55690-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,9 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55690-98:
(7*5)+(6*5)+(5*6)+(4*9)+(3*0)+(2*9)+(1*8)=157
157 % 10 = 7
So 55690-98-7 is a valid CAS Registry Number.

55690-98-7Relevant articles and documents

Synthesis of Tetraphenylstannacyclopentadienes (Stannoles). 1. Alkylation of 1,1-Dihalostannoles Leading to Lithium 1,1-Bis(η1-cyclopentadienyl)-1-halo-2,3,4,5-tetraphenylstannole, an - Anion with Pseudorotating Axial- and Equ

Gustavson, W. A.,Principe, L. M.,Rhee, W.-Z. Min,Zuckerman, J. J.

, p. 4126 - 4131 (1981)

1,1-Dibromo- and 1,1-diiodo-2,3,4,5-tetraphenylstannacyclopentadienes (dibromo- and diiodostannoles) formed from controlled phenyltin cleavage of hexaphenylstannole by elemental bromine and iodine, respectively, undergo conventional alkylation by methylli

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