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1,2,2-trimethyl-1,2-diphenyl-1-(piperidinomethyl)disilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1220959-42-1 Structure
  • Basic information

    1. Product Name: 1,2,2-trimethyl-1,2-diphenyl-1-(piperidinomethyl)disilane
    2. Synonyms: 1,2,2-trimethyl-1,2-diphenyl-1-(piperidinomethyl)disilane
    3. CAS NO:1220959-42-1
    4. Molecular Formula:
    5. Molecular Weight: 353.655
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1220959-42-1.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: 1,2,2-trimethyl-1,2-diphenyl-1-(piperidinomethyl)disilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,2-trimethyl-1,2-diphenyl-1-(piperidinomethyl)disilane(1220959-42-1)
    11. EPA Substance Registry System: 1,2,2-trimethyl-1,2-diphenyl-1-(piperidinomethyl)disilane(1220959-42-1)
  • 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: 1220959-42-1(Hazardous Substances Data)

1220959-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1220959-42-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,0,9,5 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1220959-42:
(9*1)+(8*2)+(7*2)+(6*0)+(5*9)+(4*5)+(3*9)+(2*4)+(1*2)=141
141 % 10 = 1
So 1220959-42-1 is a valid CAS Registry Number.

1220959-42-1Downstream Products

1220959-42-1Relevant articles and documents

The competition between Si-Si and Si-C cleavage in functionalised oligosilanes: Their reactivity with elemental lithium

Daeschlein, Christian,Strohmann, Carsten

, p. 2062 - 2069 (2010)

The reaction of aryl-substituted disilanes with elemental lithium is a common method for the preparation of lithiosilanes and the subsequent synthesis of functionalised oligosilanes, especially of enantiomerically pure compounds. A series of alkyl- and arylsubstituted di- and trisilanes has been investigated with respect to their reactivity against elemental lithium. Thereby, depending on the substituents, silicon-silicon bond cleavage of the central Si-Si unit and/or silicon-carbon bond cleavage to arenes are observed. Quantum chemical studies provide a deeper insight into the ongoing processes. The reactive centre can be estimated by both, bond elongation after electron transfer and frontier orbital interactions (π-bonding and σ-antibonding part). Aromatic substituents at the silicon atoms proved to be necessary for the processing of any cleavage reaction in the studied systems by stabilising the radical anion after electron transfer at the corresponding di- or trisilane. Yet, selective cleavage reactions do not depend on the number of arenes.

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