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1-[2',3',5'-tri-O-(4-toluoyl)-β-D-ribofuranosyl]-thymine-3',5'(R/S)-2H2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 219569-02-5 Structure
  • Basic information

    1. Product Name: 1-[2',3',5'-tri-O-(4-toluoyl)-β-D-ribofuranosyl]-thymine-3',5'(R/S)-2H2
    2. Synonyms:
    3. CAS NO:219569-02-5
    4. Molecular Formula:
    5. Molecular Weight: 614.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219569-02-5.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: 1-[2',3',5'-tri-O-(4-toluoyl)-β-D-ribofuranosyl]-thymine-3',5'(R/S)-2H2(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[2',3',5'-tri-O-(4-toluoyl)-β-D-ribofuranosyl]-thymine-3',5'(R/S)-2H2(219569-02-5)
    11. EPA Substance Registry System: 1-[2',3',5'-tri-O-(4-toluoyl)-β-D-ribofuranosyl]-thymine-3',5'(R/S)-2H2(219569-02-5)
  • 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: 219569-02-5(Hazardous Substances Data)

219569-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219569-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,5,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 219569-02:
(8*2)+(7*1)+(6*9)+(5*5)+(4*6)+(3*9)+(2*0)+(1*2)=155
155 % 10 = 5
So 219569-02-5 is a valid CAS Registry Number.

219569-02-5Upstream product

219569-02-5Relevant articles and documents

Synthesis of partially-deuterated 2'-deoxyribonucleoside blocks and their incorporation into an oligo-DNA for simplification of overcrowding and selective enhancement of resolution and sensitivity in the 1H-NMR spectra

Foeldesi, Andras,Maltseva, Tatiana V.,Dinya, Zoltan,Chattopadhyaya, Jyoti

, p. 14487 - 14514 (1998)

The chemical synthesis of appropriately protected partially-deuterated 2'(R/S),3',5'(R/S)-2H3-2'-deoxyribonucleoside blocks [~43 atoms % 2H at C5'(R), ~57 atom % 2H at C5'(S); ~15 atom % 2H at C2'(R), ~85 atom % 2H at C2'(S) and >99 atom % 2H at C3'] is reported. The availability of these deuterium labelled blocks on large scale has enabled the chemical assemblage of the deuterio isotopomeric 12mer [d(C1G2C3G4A5A6T7T8C9G10C11G12)]2 DNA duplex by standard solid-phase synthesis protocol in order to demonstrate the usefulness of the new 'NMR-window III' approach.

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