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78485-08-2

3,5-diphenyl-3-methyl-1,2-dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78485-08-2 Structure

  • Basic information

    1. Product Name: 3,5-diphenyl-3-methyl-1,2-dioxolane
    2. Synonyms: 3,5-diphenyl-3-methyl-1,2-dioxolane
    3. CAS NO:78485-08-2
    4. Molecular Formula:
    5. Molecular Weight: 240.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78485-08-2.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: 3,5-diphenyl-3-methyl-1,2-dioxolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-diphenyl-3-methyl-1,2-dioxolane(78485-08-2)
    11. EPA Substance Registry System: 3,5-diphenyl-3-methyl-1,2-dioxolane(78485-08-2)

  • 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: 78485-08-2(Hazardous Substances Data)

78485-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78485-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,8 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78485-08:
(7*7)+(6*8)+(5*4)+(4*8)+(3*5)+(2*0)+(1*8)=172
172 % 10 = 2
So 78485-08-2 is a valid CAS Registry Number.

78485-08-2Relevant articles and documents

SYNTHESIS AND DECOMPOSITION OF E- AND Z-3,3,5-TRISUBSTITUTED 1,2-DIOXOLANES.

Yoshida,Miura,Nojima,Kusabayashi

, p. 6279 - 6285 (2007/10/02)

The reactions of a number of ozonides and olefins in the presence of boron trifluoride-diethyl ether gave the corresponding mixtures of (E)- and (Z)-1,2-dioxolanes in 12-70% yield. The decomposition of the E-Z isomeric 1,2-dioxolanes 3a-c was undertaken under a variety of conditions, i. e. , thermal, TiCl//4-mediated, FeSO//4-catalyzed, and LiAlH//4-mediated decompositions.

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