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CAS

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412011-35-9

6-vinyl-3-cyclohexene-1-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 412011-35-9 Structure

  • Basic information

    1. Product Name: 6-vinyl-3-cyclohexene-1-carbaldehyde
    2. Synonyms:
    3. CAS NO:412011-35-9
    4. Molecular Formula:
    5. Molecular Weight: 136.194
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 412011-35-9.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-vinyl-3-cyclohexene-1-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-vinyl-3-cyclohexene-1-carbaldehyde(412011-35-9)
    11. EPA Substance Registry System: 6-vinyl-3-cyclohexene-1-carbaldehyde(412011-35-9)

  • 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: 412011-35-9(Hazardous Substances Data)

412011-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 412011-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,0,1 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 412011-35:
(8*4)+(7*1)+(6*2)+(5*0)+(4*1)+(3*1)+(2*3)+(1*5)=69
69 % 10 = 9
So 412011-35-9 is a valid CAS Registry Number.

412011-35-9Relevant articles and documents

Studies in iridoid synthesis. Chemoselective transformations of cis-1,2,4,6-tetrahydrophthalic anhydride

Stevens, Anne T.,Bull, James R.,Chibale, Kelly

, p. 586 - 595 (2008)

In the course of synthetic studies towards the development of diastereoselective routes to secoiridoid aglycones, cis-1,2,4,6- tetrahydrophthalic anhydride was transformed into the corresponding lactone cis-3a,4,7,7a-tetrahydro-3H-isobenzofuran-1-one, whi

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