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[ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 503173-77-1 Structure
  • Basic information

    1. Product Name: [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine
    2. Synonyms: [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine
    3. CAS NO:503173-77-1
    4. Molecular Formula:
    5. Molecular Weight: 522.443
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 503173-77-1.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: [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine(503173-77-1)
    11. EPA Substance Registry System: [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)adenine(503173-77-1)
  • 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: 503173-77-1(Hazardous Substances Data)

503173-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503173-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,1,7 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 503173-77:
(8*5)+(7*0)+(6*3)+(5*1)+(4*7)+(3*3)+(2*7)+(1*7)=121
121 % 10 = 1
So 503173-77-1 is a valid CAS Registry Number.

503173-77-1Relevant articles and documents

Chemical synthesis of 13C labeled anti-HIV nucleosides as mass-internal standards

Saito, Yoshio,Zevaco, Thomas A,Agrofoglio, Luigi A

, p. 9593 - 9603 (2007/10/03)

Synthesis of [13C5]-labeled anti-HIV nucleosides, e.g. d4T, ddI, ddA, is described. The methodology used has been optimized due to the very high cost of the starting compound. The key step of this approach was the stereoselective dehomologation of 1,2:5,6-di-O-isopropylidene-3-oxo-α-D-glucofuranose (2) with periodic acid and sodium borohydride, which gave optically pure ribose derivative as the exclusive product. Nucleoside derivatives 6a-c were obtained from ribosylation of 5 with persilylated nucleobases under Vorbru?ggen conditions. Deoxygenation of 9a-c under Corey-Winter conditions afforded the desired labeled nucleoside analogues 12a-c.

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