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1388771-66-1

5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-4-pyrene β-deoxynucleoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1388771-66-1 Structure

  • Basic information

    1. Product Name: 5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-4-pyrene β-deoxynucleoside
    2. Synonyms: 5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-4-pyrene β-deoxynucleoside
    3. CAS NO:1388771-66-1
    4. Molecular Formula:
    5. Molecular Weight: 662.782
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1388771-66-1.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: 5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-4-pyrene β-deoxynucleoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-4-pyrene β-deoxynucleoside(1388771-66-1)
    11. EPA Substance Registry System: 5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-4-pyrene β-deoxynucleoside(1388771-66-1)

  • 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: 1388771-66-1(Hazardous Substances Data)

1388771-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1388771-66-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,8,7,7 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1388771-66:
(9*1)+(8*3)+(7*8)+(6*8)+(5*7)+(4*7)+(3*1)+(2*6)+(1*6)=221
221 % 10 = 1
So 1388771-66-1 is a valid CAS Registry Number.

1388771-66-1Downstream Products

1388771-66-1Relevant articles and documents

Polymerase incorporation of pyrene-nucleoside triphosphates

Hollenstein, Marcel,Wojciechowski, Filip,Leumann, Christian J.

, p. 4428 - 4430 (2012)

Pyrene-deoxynucleoside triphosphates (dPTPs), varying by the positioning of the aromatic system, were synthesized. Their ability to function as substrates for the Klenow fragment of Escherichia coli DNA polymerase I and the TdT polymerase was assessed. The dPTPs are all equally well tolerated by the Klenow fragment, and lead to elongation of up to 5 extra nucleotides of a ssDNA primer in a TdT-mediated reaction. The tailing efficiency of the dPTPs compares favorably to other less drastically modified dNTPs.

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