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85972-28-7

Ethanone, 1-(3,4-diiodo-1,3-cyclohexadien-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85972-28-7 Structure

  • Basic information

    1. Product Name: Ethanone, 1-(3,4-diiodo-1,3-cyclohexadien-1-yl)-
    2. Synonyms:
    3. CAS NO:85972-28-7
    4. Molecular Formula: C8H8I2O
    5. Molecular Weight: 373.96
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85972-28-7.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: Ethanone, 1-(3,4-diiodo-1,3-cyclohexadien-1-yl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(3,4-diiodo-1,3-cyclohexadien-1-yl)-(85972-28-7)
    11. EPA Substance Registry System: Ethanone, 1-(3,4-diiodo-1,3-cyclohexadien-1-yl)-(85972-28-7)

  • 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: 85972-28-7(Hazardous Substances Data)

85972-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85972-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,7 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85972-28:
(7*8)+(6*5)+(5*9)+(4*7)+(3*2)+(2*2)+(1*8)=177
177 % 10 = 7
So 85972-28-7 is a valid CAS Registry Number.

85972-28-7Downstream Products

85972-28-7Relevant articles and documents

Preparation and Diels-Alder Reactivity of Several New Chalcogen-Halogen Substituted Butadienes

Bridges, Alexander J.,Fischer, John W.

, p. 2954 - 2961 (2007/10/02)

Addition of halogens and pseudohalogens across one ?-bond of 1,4-dichlorobut-2-yne, followed by a 1,4-elimination, is an efficient synthesis of several new polysubstituted butadienes.If the product dienes have a sulfur or selenium substituent they are quite reactive, undergoing cycloaddition with the moderately reactive dienophile methyl vinyl ketone at 20 deg C in the presence of boron trifluoride etherate.The regiochemistry of the cycloadditions was elucidated, and the limitations of the methodology are discussed.

THE DIELS-ALDER REACTIVITY OF SOME NEW SULFUR (SELENIUM) SUBSTITUTED HALOBUTADIENES

Bridges, Alexander J.,Fischer, John W.

, p. 447 - 450 (2007/10/02)

3-PhS(e)-(1),2-(di)halobutadienes undergo BF3 catalysed cycloadditions with methyl vinyl ketone at 25 deg C, to give good yields of adducts in which the regiochemistry of addition is mainly controlled by the sulfur (selenium) atom.

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