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CAS

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172039-05-3

1,2-di-O-acetyl-5-azido-5-deoxy-3-O-p-toluenesulfonyl-D-xylofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 172039-05-3 Structure

  • Basic information

    1. Product Name: 1,2-di-O-acetyl-5-azido-5-deoxy-3-O-p-toluenesulfonyl-D-xylofuranose
    2. Synonyms:
    3. CAS NO:172039-05-3
    4. Molecular Formula:
    5. Molecular Weight: 413.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172039-05-3.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-di-O-acetyl-5-azido-5-deoxy-3-O-p-toluenesulfonyl-D-xylofuranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-di-O-acetyl-5-azido-5-deoxy-3-O-p-toluenesulfonyl-D-xylofuranose(172039-05-3)
    11. EPA Substance Registry System: 1,2-di-O-acetyl-5-azido-5-deoxy-3-O-p-toluenesulfonyl-D-xylofuranose(172039-05-3)

  • 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: 172039-05-3(Hazardous Substances Data)

172039-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172039-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,0,3 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 172039-05:
(8*1)+(7*7)+(6*2)+(5*0)+(4*3)+(3*9)+(2*0)+(1*5)=113
113 % 10 = 3
So 172039-05-3 is a valid CAS Registry Number.

172039-05-3Relevant articles and documents

Synthesis and reactions of 1-(5-azido-5-deoxy-3-O-p-toluenesulfonyl-β-D-xylofuranosyl) derivatives of 5-alkyl- and 5-halo-pyrimidines

Al-Masoudi, Najim A.,Pfleiderer, W.

, p. 95 - 106 (1995)

Chemical syntheses of 1-(2-O-acetyl-5-azido--5-deoxy-3-O-p-toluenesulfonyl-β-D-xylofuranosyl)-5-iodo,- -5-fluoro-, and -5-trifluoromethyl-uracil nucleosides (11-13) as well as the thymine analogue 10 were performed from a sugar precursor and the correspon

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