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CAS

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215436-53-6

cis-2-benzoyloxymethyl-4-(N4'-acetylcytosin-1'-yl)-1,3-oxathiolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 215436-53-6 Structure

  • Basic information

    1. Product Name: cis-2-benzoyloxymethyl-4-(N4'-acetylcytosin-1'-yl)-1,3-oxathiolane
    2. Synonyms:
    3. CAS NO:215436-53-6
    4. Molecular Formula:
    5. Molecular Weight: 375.405
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215436-53-6.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: cis-2-benzoyloxymethyl-4-(N4'-acetylcytosin-1'-yl)-1,3-oxathiolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-2-benzoyloxymethyl-4-(N4'-acetylcytosin-1'-yl)-1,3-oxathiolane(215436-53-6)
    11. EPA Substance Registry System: cis-2-benzoyloxymethyl-4-(N4'-acetylcytosin-1'-yl)-1,3-oxathiolane(215436-53-6)

  • 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: 215436-53-6(Hazardous Substances Data)

215436-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215436-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,4,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 215436-53:
(8*2)+(7*1)+(6*5)+(5*4)+(4*3)+(3*6)+(2*5)+(1*3)=116
116 % 10 = 6
So 215436-53-6 is a valid CAS Registry Number.

215436-53-6Relevant articles and documents

A new strategy for the asymmetric synthesis of 1,3-oxathiolane-based nucleoside analogues

Caputo, Romualdo,Guaragna, Annalisa,Palumbo, Giovanni,Pedatella, Silvana

, p. 1455 - 1458 (2007/10/03)

A ready asymmetric synthesis of 3'-oxathionucleosides has been accomplished in three main steps from benzoyloxyethanal. The synthesis is characterized by high overall yield and considerable enantiomeric excesses. It represents a general synthetic path to prepare a wide range of heterosubstituted sulfur-containing nucleoside analogues.

Asymmetric synthesis of optically active 1,3-oxathiolane nucleoside analogues

Caputo, Romualdo,Guaragna, Annalisa,Palumbo, Giovanni,Pedatella, Silvana

, p. 1739 - 1745 (2007/10/03)

A ready asymmetric synthesis of 3'-oxa-4'-thionucleosides has been accomplished in three main steps from benzoyloxyethanal. The synthesis is characterized by high overall yield and appreciable enantiomeric excesses. It represents a general synthetic scheme to prepare a wide range of heterosubstituted sulfur-containing nucleoside analogues.

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