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(1R,3R,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(cytosin-1-yl)-2,6-dioxabicyclo<3.2.1>octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 229469-49-2 Structure
  • Basic information

    1. Product Name: (1R,3R,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(cytosin-1-yl)-2,6-dioxabicyclo<3.2.1>octane
    2. Synonyms:
    3. CAS NO:229469-49-2
    4. Molecular Formula:
    5. Molecular Weight: 505.527
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 229469-49-2.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: (1R,3R,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(cytosin-1-yl)-2,6-dioxabicyclo<3.2.1>octane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3R,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(cytosin-1-yl)-2,6-dioxabicyclo<3.2.1>octane(229469-49-2)
    11. EPA Substance Registry System: (1R,3R,4R,8S)-1-acetoxymethyl-8-benzyloxy-3-(cytosin-1-yl)-2,6-dioxabicyclo<3.2.1>octane(229469-49-2)
  • 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: 229469-49-2(Hazardous Substances Data)

229469-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229469-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,4,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 229469-49:
(8*2)+(7*2)+(6*9)+(5*4)+(4*6)+(3*9)+(2*4)+(1*9)=172
172 % 10 = 2
So 229469-49-2 is a valid CAS Registry Number.

229469-49-2Downstream Products

229469-49-2Relevant articles and documents

Conformationally locked nucleosides. Synthesis and stereochemical assignments of 2'-C,4'-C-bridged bicyclonucleosides

Wang, Guangyi,Girardet, Jean-Luc,Gunic, Esmir

, p. 7707 - 7724 (2007/10/03)

1-α-O-Methyl-3-O,5-O-TIPDS-arabinose was converted, in multiple steps, to 2,6-dioxabicyclo[3,2,1]octane derivatives, which were condensed with silylated nucleoside bases to give the desired 2',4'-bridged bicyclonucleosides. In this article, synthesis and stereochemical assignments of the bicyclonucleosides are described.

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