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156793-45-2

3'-O-tert-Butyldiphenylsilyl-5'-iodo-5'-deoxythymidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156793-45-2 Structure

  • Basic information

    1. Product Name: 3'-O-tert-Butyldiphenylsilyl-5'-iodo-5'-deoxythymidine
    2. Synonyms: 3'-O-tert-Butyldiphenylsilyl-5'-iodo-5'-deoxythymidine
    3. CAS NO:156793-45-2
    4. Molecular Formula:
    5. Molecular Weight: 590.533
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156793-45-2.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: 3'-O-tert-Butyldiphenylsilyl-5'-iodo-5'-deoxythymidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3'-O-tert-Butyldiphenylsilyl-5'-iodo-5'-deoxythymidine(156793-45-2)
    11. EPA Substance Registry System: 3'-O-tert-Butyldiphenylsilyl-5'-iodo-5'-deoxythymidine(156793-45-2)

  • 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: 156793-45-2(Hazardous Substances Data)

156793-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156793-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156793-45:
(8*1)+(7*5)+(6*6)+(5*7)+(4*9)+(3*3)+(2*4)+(1*5)=172
172 % 10 = 2
So 156793-45-2 is a valid CAS Registry Number.

156793-45-2Relevant articles and documents

Synthesis of a new hydroxyamino linked thymidine dimer via a radical C-C bond formation

Sanghvi,Cook

, p. 859 - 862 (1995)

An efficient synthesis of a thymidine nucleoside dimer [T-3'-β-O- N(CH3)-CH2-5'-T] has been accomplished via an intermolecular radical coupling reaction. The novel dimer contains an achiral and neutral backbone linkage which may have potential application in constructing backbone modified antisense oligonucleosides.

Four step synthesis of a 5′-deoxy-5′-iodomethylthymidine

Baeschlin, Daniel K.,Daube, Michael,Blaettler, Monika O.,Benner, Steven A.,Richert, Clemens

, p. 1591 - 1592 (2007/10/03)

The conversion of an alkylsulfonate to an iodide with triphenylphosphine/iodine in benzene has been performed for a nucleoside. Starting from thymidine, 3′-protected 5′-deoxy-5′-iodomethylthymidine was synthesized in 4 steps.

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