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2-Propanone, 1-(2-cyclohexen-1-yloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65755-86-4 Structure
  • Basic information

    1. Product Name: 2-Propanone, 1-(2-cyclohexen-1-yloxy)-
    2. Synonyms:
    3. CAS NO:65755-86-4
    4. Molecular Formula: C9H14O2
    5. Molecular Weight: 154.209
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65755-86-4.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-Propanone, 1-(2-cyclohexen-1-yloxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propanone, 1-(2-cyclohexen-1-yloxy)-(65755-86-4)
    11. EPA Substance Registry System: 2-Propanone, 1-(2-cyclohexen-1-yloxy)-(65755-86-4)
  • 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: 65755-86-4(Hazardous Substances Data)

65755-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65755-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,5 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65755-86:
(7*6)+(6*5)+(5*7)+(4*5)+(3*5)+(2*8)+(1*6)=164
164 % 10 = 4
So 65755-86-4 is a valid CAS Registry Number.

65755-86-4Relevant articles and documents

Regiospecific Synthesis of β, γ-Unsaturated Ketones from Allylic Alcohols. Claisen Rearrangement of α-Allyloxy Ketone Enol Derivatives

Kachinsky, Joseph L. C.,Salomon, Robert G.

, p. 1393 - 1401 (2007/10/02)

β,γ-Unsaturated ketones are prepared with regiospecific C-C bond formation at the former γ-position of primary, secondary, or tertiary allylic alcohol precursors by a process involving sigmatropic Claisen rearrangement of intermediate α-allyloxy ket

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