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methoxyethane; protonated form is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52067-06-8 Structure
  • Basic information

    1. Product Name: methoxyethane; protonated form
    2. Synonyms: methoxyethane; protonated form
    3. CAS NO:52067-06-8
    4. Molecular Formula:
    5. Molecular Weight: 61.1039
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52067-06-8.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: methoxyethane; protonated form(CAS DataBase Reference)
    10. NIST Chemistry Reference: methoxyethane; protonated form(52067-06-8)
    11. EPA Substance Registry System: methoxyethane; protonated form(52067-06-8)
  • 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: 52067-06-8(Hazardous Substances Data)

52067-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52067-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,6 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52067-06:
(7*5)+(6*2)+(5*0)+(4*6)+(3*7)+(2*0)+(1*6)=98
98 % 10 = 8
So 52067-06-8 is a valid CAS Registry Number.

52067-06-8Downstream Products

52067-06-8Relevant articles and documents

Chloronium Ions as Alkylating Agents in the Gas-Phase Ion-Molecule Reactions with Negative Temperature Dependence

Sharma, D. K. Sen,Kebarle, P.

, p. 19 - 24 (1982)

The kinetics of the reactions Me2Cl+ + B = MeB+ + MeCl and MeEtCl+ + B = MeB+ or (EtB+) + EtCl (or MeCl) were studied with a pulsed-electron-beam, high-pressure mass spectrometer.At room temperature the rate constants were found to increase in the order B = benzene, toluene, isopropylbenzene, EtOH, Me2O, Et2O.At this point k become equal to the orbiting capture rate constant k1 ca. 10-9 molecule-1 cm3 s-.NH3 and Me3N were alkylated at orbiting capture rates.The temperature dependence of the rate constants for B = toluene, Me2O, and Et2O was examined.The rate constants were found to increase with decrease of temperature.This increase continued until the rate constants reached the magnitude of the orbiting rate constant kL.The rates remained approximately independent of temperature below this temperature.At low temperatures the collision-stabilized Me2Cl+B and MeEtCl+B could be observed.The temperature dependence of the equilibrium Me2Cl+ + toluene = (Me2Cl-toluene)+ was measured and led to the corresponding ΔHo and ΔSo.The reaction Me2Cl+ + benzene = Me-benzene+ + MeCl was found to have positive temperature dependence.On the basis of the above data it is suggested that the reactions Me2Cl+ + B = MeB+ + MeCl have an internal barrier in the potential energy of the reaction coordinate.This barrier protrudes above the energy level of the reactants (Me2Cl+ + B) for B = benzene.This leads to positive temperature dependence.For all other B, the top of the internal barrier lies below the level of the reactants and sinks lower, roughly in the order of increasing basicity of B.This lead to negative temperature dependence (toluene, isopropylbenzene, Me2O, Et2O).For B = NH3, MeNH2, Me3N, the barrier is so low that the reactions have orbiting capture rates equal to kL.Alkylation of bases B by chloronium ions like Me2Cl+ might have considerable utility in mass spectrometric analysis by chemical ionization.Ethers can be distinguished from alcohols and tertiary amines from primary and secondary amines.The alkylated ethers and the tertiary amines have no protic hydrogens and therefore do not form strongly hydrogen-bonded adducts.

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