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CAS

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333335-49-2

2-acetoxy-4-benzoyloxymethylterahydrofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 333335-49-2 Structure

  • Basic information

    1. Product Name: 2-acetoxy-4-benzoyloxymethylterahydrofuran
    2. Synonyms: 2-acetoxy-4-benzoyloxymethylterahydrofuran
    3. CAS NO:333335-49-2
    4. Molecular Formula:
    5. Molecular Weight: 264.278
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 333335-49-2.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: 2-acetoxy-4-benzoyloxymethylterahydrofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetoxy-4-benzoyloxymethylterahydrofuran(333335-49-2)
    11. EPA Substance Registry System: 2-acetoxy-4-benzoyloxymethylterahydrofuran(333335-49-2)

  • 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: 333335-49-2(Hazardous Substances Data)

333335-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333335-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,3 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 333335-49:
(8*3)+(7*3)+(6*3)+(5*3)+(4*3)+(3*5)+(2*4)+(1*9)=122
122 % 10 = 2
So 333335-49-2 is a valid CAS Registry Number.

333335-49-2Relevant articles and documents

Regioselective alkylation of guanines using 2-acetoxytetrahydrofurans

Geen, Graham R.,Kincey, Peter M.,Spoors, P. Grant

, p. 1781 - 1784 (2007/10/03)

Reaction of silylated guanine derivatives with 2-acetoxy-4-benzoyloxymethyltetrahydrofuran in DMF or NMP resulted in selective N-9 alkylation. This was used as the basis for a regioselective synthesis of the anti-viral agents famciclovir and penciclovir.

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