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CAS

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241819-88-5

(2,4,6-tris[bis(trimethylsilyl)methyl]phenyl)[bis(trimethylsilyl)methyl]iodomethylplumbane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 241819-88-5 Structure

  • Basic information

    1. Product Name: (2,4,6-tris[bis(trimethylsilyl)methyl]phenyl)[bis(trimethylsilyl)methyl]iodomethylplumbane
    2. Synonyms:
    3. CAS NO:241819-88-5
    4. Molecular Formula:
    5. Molecular Weight: 1060.82
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 241819-88-5.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: (2,4,6-tris[bis(trimethylsilyl)methyl]phenyl)[bis(trimethylsilyl)methyl]iodomethylplumbane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2,4,6-tris[bis(trimethylsilyl)methyl]phenyl)[bis(trimethylsilyl)methyl]iodomethylplumbane(241819-88-5)
    11. EPA Substance Registry System: (2,4,6-tris[bis(trimethylsilyl)methyl]phenyl)[bis(trimethylsilyl)methyl]iodomethylplumbane(241819-88-5)

  • 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: 241819-88-5(Hazardous Substances Data)

241819-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 241819-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,8,1 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 241819-88:
(8*2)+(7*4)+(6*1)+(5*8)+(4*1)+(3*9)+(2*8)+(1*8)=145
145 % 10 = 5
So 241819-88-5 is a valid CAS Registry Number.

241819-88-5Downstream Products

241819-88-5Relevant articles and documents

Synthesis, structure, and reactivity of kinetically stabilized divalent organolead compounds (plumbylenes)

Kano, Naokazu,Shibata, Kazusato,Tokitoh, Norihiro,Okazaki, Renji

, p. 2999 - 3007 (2008/10/08)

Divalent organolead compounds (plumbylenes; Tip2Pb (6; Tip = 2,4,6-triisopropylphenyl) and Tbt(R)Pb (7a, R = Tbt; Tb, R = Ttm; 7c, R = Tip; 7d, R = Dis; Tbt = 2,4,6-tris[bis-(trimethylsilyl)methyl]phenyl, Ttm = 2,4,6-tris[(trimethylsilyl)methyl]phenyl, and Dis = bis-(trimethylsilyl)methyl)) were synthesized by taking advantage of kinetic stabilization afforded by bulky substituents and characterized by UV/vis and 207Pb NMR spectroscopy. X-ray structural analysis revealed that plumbylene 7a has a V-shaped, monomeric structure. Reactions of these plumbylenes with methyl iodide, carbon tetrabromide, diphenyl disulfide, diphenyl diselenide, and elemental sulfur are described. New methods for the synthesis of plumbylenes from tetravalent organolead compounds, by reductive debromination of dibromoplumbanes and exhaustive desulfurization of tetrathiaplumbolanes, were developed.

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