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156569-33-4

6-(2-benzyloxyethyl)-1,5-dimethyl-4-methoxypyrimidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 6-(2-benzyloxyethyl)-1,5-dimethyl-4-methoxypyrimidin-2-one

    Cas No: 156569-33-4

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  • 156569-33-4 Structure

  • Basic information

    1. Product Name: 6-(2-benzyloxyethyl)-1,5-dimethyl-4-methoxypyrimidin-2-one
    2. Synonyms:
    3. CAS NO:156569-33-4
    4. Molecular Formula:
    5. Molecular Weight: 288.346
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156569-33-4.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: 6-(2-benzyloxyethyl)-1,5-dimethyl-4-methoxypyrimidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(2-benzyloxyethyl)-1,5-dimethyl-4-methoxypyrimidin-2-one(156569-33-4)
    11. EPA Substance Registry System: 6-(2-benzyloxyethyl)-1,5-dimethyl-4-methoxypyrimidin-2-one(156569-33-4)

  • 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: 156569-33-4(Hazardous Substances Data)

156569-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156569-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,5,6 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156569-33:
(8*1)+(7*5)+(6*6)+(5*5)+(4*6)+(3*9)+(2*3)+(1*3)=164
164 % 10 = 4
So 156569-33-4 is a valid CAS Registry Number.

156569-33-4Relevant articles and documents

Synthesis of C-6 pyrimidine acyclic nucleoside analogs as potential antiviral agents

Hsu,Wise,Shannon,Drach,Townsend

, p. 563 - 584 (2007/10/02)

A number of pyrimidine acyclic nucleosides in which the acyclic moiety is attached to the C-6 position rather than N-1 of the pyrimidine ring have been prepared. This was accomplished via treatment of lithiated 2,4-dimethoxy- 5,6-dimethylpyrimidine, or, 2

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