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1-(1-C-cyano-2-deoxy-3,5-di-O-t-butyldimethylsilyl-β-D-erythro-pentofuranosyl)thymine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 167023-17-8 Structure
  • Basic information

    1. Product Name: 1-(1-C-cyano-2-deoxy-3,5-di-O-t-butyldimethylsilyl-β-D-erythro-pentofuranosyl)thymine
    2. Synonyms: 1-(1-C-cyano-2-deoxy-3,5-di-O-t-butyldimethylsilyl-β-D-erythro-pentofuranosyl)thymine
    3. CAS NO:167023-17-8
    4. Molecular Formula:
    5. Molecular Weight: 495.767
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 167023-17-8.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-(1-C-cyano-2-deoxy-3,5-di-O-t-butyldimethylsilyl-β-D-erythro-pentofuranosyl)thymine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1-C-cyano-2-deoxy-3,5-di-O-t-butyldimethylsilyl-β-D-erythro-pentofuranosyl)thymine(167023-17-8)
    11. EPA Substance Registry System: 1-(1-C-cyano-2-deoxy-3,5-di-O-t-butyldimethylsilyl-β-D-erythro-pentofuranosyl)thymine(167023-17-8)
  • 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: 167023-17-8(Hazardous Substances Data)

167023-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167023-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,0,2 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167023-17:
(8*1)+(7*6)+(6*7)+(5*0)+(4*2)+(3*3)+(2*1)+(1*7)=118
118 % 10 = 8
So 167023-17-8 is a valid CAS Registry Number.

167023-17-8Downstream Products

167023-17-8Relevant articles and documents

Synthesis and biological evaluation of 1′-C-cyano-pyrimidine nucleosides

Yoshimura, Yuichi,Kano, Fumitaka,Miyazaki, Shuichi,Ashida, Noriyuki,Sakata, Shinji,Haraguchi, Kazuhiro,Itoh, Yoshiharu,Tanaka, Hiromichi,Miyasaka, Tadashi

, p. 305 - 324 (1996)

2′-Deoxy-, 2′-bromo-, and arabino-1′-C-cyano-pyrimidine nucleosides were synthesized from O2,2′-cyclouridine. Incorporation of cyano group at the anomeric position was achieved by treatment of 1′,2′-unsaturated uridine with NBS in the presence of pivalic acid followed by TMS-cyanide and stannic chloride. Antineoplastic and antiviral activities of those compounds are also discussed.

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