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CAS

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134967-25-2

1-(2-hexa-1,5-dienyl)-1-methyl-2,5-bis(methylene)stannolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134967-25-2 Structure

  • Basic information

    1. Product Name: 1-(2-hexa-1,5-dienyl)-1-methyl-2,5-bis(methylene)stannolane
    2. Synonyms: 1-(2-hexa-1,5-dienyl)-1-methyl-2,5-bis(methylene)stannolane
    3. CAS NO:134967-25-2
    4. Molecular Formula:
    5. Molecular Weight: 295.012
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134967-25-2.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: 1-(2-hexa-1,5-dienyl)-1-methyl-2,5-bis(methylene)stannolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-hexa-1,5-dienyl)-1-methyl-2,5-bis(methylene)stannolane(134967-25-2)
    11. EPA Substance Registry System: 1-(2-hexa-1,5-dienyl)-1-methyl-2,5-bis(methylene)stannolane(134967-25-2)

  • 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: 134967-25-2(Hazardous Substances Data)

134967-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134967-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,6 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134967-25:
(8*1)+(7*3)+(6*4)+(5*9)+(4*6)+(3*7)+(2*2)+(1*5)=152
152 % 10 = 2
So 134967-25-2 is a valid CAS Registry Number.

134967-25-2Downstream Products

134967-25-2Relevant articles and documents

Formation of organodilithium compounds via lithium-tin exchange

Ashe III, Arthur J.,Lohr, Lawrence L.,Al-Taweel, Samir M.

, p. 2424 - 2431 (2008/10/08)

The reaction of methyllithium in THF with 2,5-bis(trimethylstannyl)-1,5-hexadiene (6) affords 2,5-dilithio-1,5-hexadiene (2) via the intermediacy of lithium stannates. The similar reaction of (2Z,4Z)-2,5-bis(trimethylstannyl)-2,4-hexadiene (11) affords (2E,4E)-2,5-dilithio-2,4-hexadiene (3). The more favorable formation of 3 suggests a greater relative stability over 2. Ab initio calculations indicate that the symmetrical dilithium-bridged structure found for 3 is more favorable than the unsymmetrical dilithium-bridged structure found for 2.

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