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CAS

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863498-62-8

2-(3'-phenylprop-1'-ynyl)cyclohex-1-ene-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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  • 863498-62-8 Structure

  • Basic information

    1. Product Name: 2-(3'-phenylprop-1'-ynyl)cyclohex-1-ene-1-carbaldehyde
    2. Synonyms: 2-(3'-phenylprop-1'-ynyl)cyclohex-1-ene-1-carbaldehyde
    3. CAS NO:863498-62-8
    4. Molecular Formula:
    5. Molecular Weight: 224.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 863498-62-8.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: 2-(3'-phenylprop-1'-ynyl)cyclohex-1-ene-1-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3'-phenylprop-1'-ynyl)cyclohex-1-ene-1-carbaldehyde(863498-62-8)
    11. EPA Substance Registry System: 2-(3'-phenylprop-1'-ynyl)cyclohex-1-ene-1-carbaldehyde(863498-62-8)

  • 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: 863498-62-8(Hazardous Substances Data)

863498-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863498-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,4,9 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 863498-62:
(8*8)+(7*6)+(6*3)+(5*4)+(4*9)+(3*8)+(2*6)+(1*2)=218
218 % 10 = 8
So 863498-62-8 is a valid CAS Registry Number.

863498-62-8Relevant articles and documents

The dipolar route to azepin-3-one derivatives by heterocyclization of linear and monocyclic enallenyl nitrones as the key step

Knobloch, Karin,Koch, Joachim,Keller, Manfred,Eberbach, Wolfgang

, p. 2715 - 2733 (2007/10/03)

The recently discovered transformation of benzopentenynyl nitrones into 1,2-dihydrobenz[c]azepin-3-ones has been extended to the synthesis of structurally different systems including the monocyclic derivatives 17 and 18, the bicyclic azepinones 10a-d, and

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