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CAS

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55177-07-6

2,2'-anhydro-1-α-D-ribofuranosylthymine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55177-07-6 Structure

  • Basic information

    1. Product Name: 2,2'-anhydro-1-α-D-ribofuranosylthymine
    2. Synonyms: 2,2'-anhydro-1-α-D-ribofuranosylthymine
    3. CAS NO:55177-07-6
    4. Molecular Formula:
    5. Molecular Weight: 240.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55177-07-6.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: 2,2'-anhydro-1-α-D-ribofuranosylthymine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2'-anhydro-1-α-D-ribofuranosylthymine(55177-07-6)
    11. EPA Substance Registry System: 2,2'-anhydro-1-α-D-ribofuranosylthymine(55177-07-6)

  • 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: 55177-07-6(Hazardous Substances Data)

55177-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55177-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,7 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55177-07:
(7*5)+(6*5)+(5*1)+(4*7)+(3*7)+(2*0)+(1*7)=126
126 % 10 = 6
So 55177-07-6 is a valid CAS Registry Number.

55177-07-6Upstream product

55177-07-6Downstream Products

55177-07-6Relevant articles and documents

Facile synthesis of α-anomeric pyrimidine nucleosides

Sawai,Nakamura,Hayashi,Shinozuka

, p. 1647 - 1654 (1994)

2-Amino-α-D-ribofurano[1',2':4,5]-2-oxazoline reacted with α- bromoacrylonitrile yielding 2,2'-anhydro-1-α-D-ribofuranosylcytosine which was converted to α-cytidine and α-2'-deoxycytidine. Reaction of 2-amino- α-D-ribofurano[1',2':4,5]-2-oxazoline and ethyl α-(bromomethyl)acrylate afforded 2,2'-anhydro-1-α-D-ribofuranosylthymine, a precursor of α- thymidine and α-ribothymidine.

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