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854920-59-5

2-[3,4-bis-benzyloxy-5-(3-methyl-but-2-enyl)-phenyl]-[1,3]dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 854920-59-5 Structure

  • Basic information

    1. Product Name: 2-[3,4-bis-benzyloxy-5-(3-methyl-but-2-enyl)-phenyl]-[1,3]dioxolane
    2. Synonyms: 2-[3,4-bis-benzyloxy-5-(3-methyl-but-2-enyl)-phenyl]-[1,3]dioxolane
    3. CAS NO:854920-59-5
    4. Molecular Formula:
    5. Molecular Weight: 430.544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 854920-59-5.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-[3,4-bis-benzyloxy-5-(3-methyl-but-2-enyl)-phenyl]-[1,3]dioxolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[3,4-bis-benzyloxy-5-(3-methyl-but-2-enyl)-phenyl]-[1,3]dioxolane(854920-59-5)
    11. EPA Substance Registry System: 2-[3,4-bis-benzyloxy-5-(3-methyl-but-2-enyl)-phenyl]-[1,3]dioxolane(854920-59-5)

  • 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: 854920-59-5(Hazardous Substances Data)

854920-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854920-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,9,2 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 854920-59:
(8*8)+(7*5)+(6*4)+(5*9)+(4*2)+(3*0)+(2*5)+(1*9)=195
195 % 10 = 5
So 854920-59-5 is a valid CAS Registry Number.

854920-59-5Relevant articles and documents

Application of benzyl protecting groups in the synthesis of prenylated aromatic compounds

Odejinmi, Sina I.,Wiemer, David F.

, p. 3871 - 3874 (2007/10/03)

Benzyl ethers have proven to be useful protecting groups for synthesis of phenols bearing isoprenoid chains because the benzyl groups can tolerate the conditions of halogen-metal exchange used to introduce the side chains yet are cleaved in good yields upon treatment with sodium s-butanol.

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