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68069-67-0

Bicyclo[2.2.2]oct-5-en-2-one, (1S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 68069-67-0 Structure

  • Basic information

    1. Product Name: Bicyclo[2.2.2]oct-5-en-2-one, (1S)-
    2. Synonyms:
    3. CAS NO:68069-67-0
    4. Molecular Formula: C8H10O
    5. Molecular Weight: 122.167
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68069-67-0.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: Bicyclo[2.2.2]oct-5-en-2-one, (1S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[2.2.2]oct-5-en-2-one, (1S)-(68069-67-0)
    11. EPA Substance Registry System: Bicyclo[2.2.2]oct-5-en-2-one, (1S)-(68069-67-0)

  • 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: 68069-67-0(Hazardous Substances Data)

68069-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68069-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68069-67:
(7*6)+(6*8)+(5*0)+(4*6)+(3*9)+(2*6)+(1*7)=160
160 % 10 = 0
So 68069-67-0 is a valid CAS Registry Number.

68069-67-0Upstream product

68069-67-0Relevant articles and documents

Fragmentation of Homoallylic Alkoxides. Thermolysis of Potassium 2-Substituted Bicyclooct-5-en-2-alkoxides

Snowden, Roger L.,Schulte-Elte, Karl H.

, p. 2193 - 2202 (2007/10/02)

Thermolysis of the potassium 2-substituted bicyclooct-5-en-2-alkoxides derived from alcohols 2-17 at 90-120 deg C in hexamethylphosphoric triamide affords unsaturated ketones resulting from allylic bond cleavage.The mechanistic and synthetic aspects of this anionic fragmentation are discussed with reference to the formation of 1-(3'-cyclohexenyl)-2-alkanones 18-28 via initial heterolytic C(1),C(2)-bond cleavage in the substrate alkoxide and regioselective, intramolecular protonation of the resultant transient allylic anion.

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