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CAS

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52417-08-0

O3',O5'-bis-(4-methoxy-trityl)-thymidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52417-08-0 Structure

  • Basic information

    1. Product Name: O3',O5'-bis-(4-methoxy-trityl)-thymidine
    2. Synonyms: O3',O5'-bis-(4-methoxy-trityl)-thymidine
    3. CAS NO:52417-08-0
    4. Molecular Formula:
    5. Molecular Weight: 786.924
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52417-08-0.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: O3',O5'-bis-(4-methoxy-trityl)-thymidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: O3',O5'-bis-(4-methoxy-trityl)-thymidine(52417-08-0)
    11. EPA Substance Registry System: O3',O5'-bis-(4-methoxy-trityl)-thymidine(52417-08-0)

  • 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: 52417-08-0(Hazardous Substances Data)

52417-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52417-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,1 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52417-08:
(7*5)+(6*2)+(5*4)+(4*1)+(3*7)+(2*0)+(1*8)=100
100 % 10 = 0
So 52417-08-0 is a valid CAS Registry Number.

52417-08-0Downstream Products

52417-08-0Relevant articles and documents

Tritylation of alcohols under mild conditions without using silver salts

Shahsavari, Shahien,Chen, Jinsen,Wigstrom, Travis,Gooding, James,Gauronskas, Alexander,Fang, Shiyue

, p. 3877 - 3880 (2016)

Secondary alcohols were conveniently tritylated under mild conditions within a short running time with tritylium trifluoroacetate generated in situ from trityl alcohols and trifluoroacetic anhydride. No expensive silver salts were needed for the reactions. Four secondary alcohols were tritylated with both mono- and dimethoxy trityl alcohols giving good to excellent isolated yields. The reaction was also tested on four nucleoside derivatives that have primary alcohols. Satisfactory results were also obtained.

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