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556074-01-2

2-cyclohexanecarbonyl-3-methoxy-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 556074-01-2 Structure

  • Basic information

    1. Product Name: 2-cyclohexanecarbonyl-3-methoxy-cyclohex-2-enone
    2. Synonyms:
    3. CAS NO:556074-01-2
    4. Molecular Formula:
    5. Molecular Weight: 236.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 556074-01-2.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-cyclohexanecarbonyl-3-methoxy-cyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-cyclohexanecarbonyl-3-methoxy-cyclohex-2-enone(556074-01-2)
    11. EPA Substance Registry System: 2-cyclohexanecarbonyl-3-methoxy-cyclohex-2-enone(556074-01-2)

  • 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: 556074-01-2(Hazardous Substances Data)

556074-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 556074-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 556074-01:
(8*5)+(7*5)+(6*6)+(5*0)+(4*7)+(3*4)+(2*0)+(1*1)=152
152 % 10 = 2
So 556074-01-2 is a valid CAS Registry Number.

556074-01-2Relevant articles and documents

Isomerization of enol esters derived from 2-acyl-1,3-cyclohexanediones: Mechanism and driving force

Liu, Hun-Ge,Wu, Chung-Shieh,Wang, Jen-Fei,Yang, Ding-Yah

, p. 3137 - 3141 (2003)

A series of 2-acyl-1,3-cyclohexanediones were prepared and isomerization mechanisms of the corresponding enol esters were investigated. The driving force for this migration is likely that the intrinsic electrostatic repulsion between the 2-acyl oxygen atom and the two 1,3-diketone oxygens caused deformation of enol esters from planarity and resulted in their high susceptibility to enolization and subsequent isomerization.

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