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431063-50-2

di(1,2,3,4,5-pentaphenyl-1-stanna-cyclopentadienyl) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 431063-50-2 Structure

  • Basic information

    1. Product Name: di(1,2,3,4,5-pentaphenyl-1-stanna-cyclopentadienyl)
    2. Synonyms: di(1,2,3,4,5-pentaphenyl-1-stanna-cyclopentadienyl)
    3. CAS NO:431063-50-2
    4. Molecular Formula:
    5. Molecular Weight: 1104.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 431063-50-2.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: di(1,2,3,4,5-pentaphenyl-1-stanna-cyclopentadienyl)(CAS DataBase Reference)
    10. NIST Chemistry Reference: di(1,2,3,4,5-pentaphenyl-1-stanna-cyclopentadienyl)(431063-50-2)
    11. EPA Substance Registry System: di(1,2,3,4,5-pentaphenyl-1-stanna-cyclopentadienyl)(431063-50-2)

  • 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: 431063-50-2(Hazardous Substances Data)

431063-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 431063-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,1,0,6 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 431063-50:
(8*4)+(7*3)+(6*1)+(5*0)+(4*6)+(3*3)+(2*5)+(1*0)=102
102 % 10 = 2
So 431063-50-2 is a valid CAS Registry Number.

431063-50-2Relevant articles and documents

Synthesis and reactions of stannole anions

Haga, Ryuta,Saito, Masaichi,Yoshioka, Michikazu

, p. 1297 - 1306 (2008/02/06)

The synthesis of stannole anions bearing various substituents on the tin atom is described. The reduction of hexaphenylstannole by the proper amount of lithium gave 1,2,3,4,5-pentaphenylstannole anion 1. The reaction of 1 with 1,n-dihaloalkanes (n = 1, 3,

Synthesis and structures of bi(1,1-stannole)s

Saito, Masaichi,Haga, Ryuta,Yoshioka, Michikazu

, p. 3750 - 3755 (2007/10/03)

The synthesis and structures of bi(1,1-stannole)s are described. Treatment of 1-bromo-4-(dibromophenylstannyl)-1,3-butadiene with tert-butyllithium gives the bi(1,1-stannole) having a phenyl group on each tin atom, whereas treatment of 1-bromo-4-(tribromostannyl)-1,3-butadiene with phenyl- or bulky alkyllithiums gives the bi(1,1-stannole) having a phenyl or an alkyl group on each tin atom. The X-ray analysis of the tert-butyl-substituted bi(1,1-stannole) is also described. All bi(1,1-stannole)s display two shoulder absorption bands due to π-π* and σ-π* transitions. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.

Formation of the first monoanion and dianion of stannole

Saito, Masaichi,Haga, Ryuta,Yoshioka, Michikazu

, p. 1002 - 1003 (2007/10/03)

The first syntheses of mono- and dianions of stannole were accomplished by transmetallation or reduction of the novel bi(1,1-stannole).

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