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1352749-75-7

C43H55N4O10P is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352749-75-7 Structure

  • Basic information

    1. Product Name: C43H55N4O10P
    2. Synonyms:
    3. CAS NO:1352749-75-7
    4. Molecular Formula:
    5. Molecular Weight: 818.904
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352749-75-7.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: C43H55N4O10P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C43H55N4O10P(1352749-75-7)
    11. EPA Substance Registry System: C43H55N4O10P(1352749-75-7)

  • 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: 1352749-75-7(Hazardous Substances Data)

1352749-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352749-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,7,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1352749-75:
(9*1)+(8*3)+(7*5)+(6*2)+(5*7)+(4*4)+(3*9)+(2*7)+(1*5)=177
177 % 10 = 7
So 1352749-75-7 is a valid CAS Registry Number.

1352749-75-7Downstream Products

1352749-75-7Relevant articles and documents

4′-Alkoxy oligodeoxynucleotides: A novel class of RNA mimics

Liboska, Radek,Snasel, Jan,Barvik, Ivan,Budesinsky, Milos,Pohl, Radek,Toik, Zdenek,Pav, Ondej,Rejman, Dominik,Novak, Pavel,Rosenberg, Ivan

, p. 8261 - 8267 (2012/04/23)

4′-Alkoxy-oligothymidylates were prepared as model compounds to study the influence of a C4′-alkoxy group on hybridisation. The phosphodiester homooligomers (15 units long) containing either a 4′-methoxy or 4′-(2-methoxyethoxy) group were found to display increased hybridisation with both dA15 and rA15 complementary counterparts compared to the natural oligothymidylate. In addition, we found their hybridisation behaviour to be similar to that of the regioisomeric 2′-O-methyl-oligothymidylate. The formed complexes (duplexes and triplexes) were studied using UV spectroscopy and polyacrylamide gel electrophoresis (PAGE). Structural background of the hybridization behaviour was examined using NMR and MDS. The favourable hybridisation properties of the 4′-alkoxyoligothymidylates indicated that 4′-alkoxy modified nucleotides are promising compounds for the assembly of chimeric oligonucleotides with tunable properties. The Royal Society of Chemistry 2011.

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