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CAS

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80754-45-6

7-syn-iodo-2-exo-methoxybicyclo<2.2.1>heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80754-45-6 Structure

  • Basic information

    1. Product Name: 7-syn-iodo-2-exo-methoxybicyclo<2.2.1>heptane
    2. Synonyms:
    3. CAS NO:80754-45-6
    4. Molecular Formula:
    5. Molecular Weight: 252.095
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80754-45-6.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: 7-syn-iodo-2-exo-methoxybicyclo<2.2.1>heptane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-syn-iodo-2-exo-methoxybicyclo<2.2.1>heptane(80754-45-6)
    11. EPA Substance Registry System: 7-syn-iodo-2-exo-methoxybicyclo<2.2.1>heptane(80754-45-6)

  • 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: 80754-45-6(Hazardous Substances Data)

80754-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80754-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,5 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80754-45:
(7*8)+(6*0)+(5*7)+(4*5)+(3*4)+(2*4)+(1*5)=136
136 % 10 = 6
So 80754-45-6 is a valid CAS Registry Number.

80754-45-6Downstream Products

80754-45-6Relevant articles and documents

Oxidatively Assisted Nucleophilic Substitution/Elimination of Alkyl Iodides in Alcoholic Media. A Further Study

Davidson, Robert I.,Kropp, Paul J.

, p. 1904 - 1909 (1982)

Oxidation of a series of alkyl halides with alcoholic 3-chloroperoxybenzoic acid afforded the results outlined in Charts I-III and Tables I-III.The reaction was found to be a powerful and convenient method for effecting nucleophilic substitution in a variety of systems, including the highly inert 1- and 7-bicycloheptyl systems.Qualitatively, the number of molar equivalents of oxidant required varied inversely with the expected ease of substitution for a given system.A mechanism is suggested whereby the iodide is oxidized stepwise to a species RIOn in which n is an integer sufficiently large that the system in question will undergo nucleophilic substitution or elimination.Reaction in the presence of added chloride or bromide ion usually resulted in a facilitation of reaction rate and a decrease in the number of molar equivalents of oxidant required; the principal product under these conditions was usually the corresponding chloride or bromide.

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