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343230-65-9

6-Phenyl-6-(tetrahydropyran-2-yloxy)fulvene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 343230-65-9 Structure

  • Basic information

    1. Product Name: 6-Phenyl-6-(tetrahydropyran-2-yloxy)fulvene
    2. Synonyms:
    3. CAS NO:343230-65-9
    4. Molecular Formula:
    5. Molecular Weight: 268.356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 343230-65-9.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: 6-Phenyl-6-(tetrahydropyran-2-yloxy)fulvene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Phenyl-6-(tetrahydropyran-2-yloxy)fulvene(343230-65-9)
    11. EPA Substance Registry System: 6-Phenyl-6-(tetrahydropyran-2-yloxy)fulvene(343230-65-9)

  • 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: 343230-65-9(Hazardous Substances Data)

343230-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343230-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,2,3 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 343230-65:
(8*3)+(7*4)+(6*3)+(5*2)+(4*3)+(3*0)+(2*6)+(1*5)=109
109 % 10 = 9
So 343230-65-9 is a valid CAS Registry Number.

343230-65-9Relevant articles and documents

Synthesis of New Fulvene Derivatives

Knight, David B.,Burnette, James C.,Hall, Randall W.,Lambeth, Gregory H.

, p. 184 - 186 (2007/10/02)

Eight new alkyl or aryl pentafulvene derivatives bearing alkyloxy substituents at C6 have been prepared by base-induced condensation of cyclopentadiene with appropriately substituted ketones.All new fulvenes were converted to Diels-Alder cycloaddition pro

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