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CAS

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448896-27-3

(R)-2-((E)-(2-phenylsulfonyl)-ethenyloxymethyl)-oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 448896-27-3 Structure

  • Basic information

    1. Product Name: (R)-2-((E)-(2-phenylsulfonyl)-ethenyloxymethyl)-oxirane
    2. Synonyms: (R)-2-((E)-(2-phenylsulfonyl)-ethenyloxymethyl)-oxirane
    3. CAS NO:448896-27-3
    4. Molecular Formula:
    5. Molecular Weight: 240.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 448896-27-3.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: (R)-2-((E)-(2-phenylsulfonyl)-ethenyloxymethyl)-oxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-((E)-(2-phenylsulfonyl)-ethenyloxymethyl)-oxirane(448896-27-3)
    11. EPA Substance Registry System: (R)-2-((E)-(2-phenylsulfonyl)-ethenyloxymethyl)-oxirane(448896-27-3)

  • 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: 448896-27-3(Hazardous Substances Data)

448896-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448896-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,8,9 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 448896-27:
(8*4)+(7*4)+(6*8)+(5*8)+(4*9)+(3*6)+(2*2)+(1*7)=213
213 % 10 = 3
So 448896-27-3 is a valid CAS Registry Number.

448896-27-3Relevant articles and documents

Synthesis and biological activity of a series of methylene-expanded oxetanocin nucleoside analogues

Jung, Michael E.,Toyota, Akemi,De Clercq, Erik,Balzarini, Jan

, p. 499 - 520 (2007/10/03)

A series of methylene-expanded oxetanocin nucleoside analogues, e.g. analogues of 2 and the known antiviral nucleosides AZT, FLT, and ddC (3) were prepared by a very direct route beginning with the readily available (S)-glycidol 4 and proceeding via the dihydrofuran-3-methanols 9a,b. Biological testing of these modified nucleosides indicates that they are non-cytotoxic compounds with generally weak antiviral activity. However, the guanosine analogue 2G showed pronounced activity vs. herpes simplex virus type 1 (HSV-1) in cell culture and was HSV-1-encoded thymidine kinase dependent. This compound is therefore an interesting new lead structure for the development of new anti-HSV agents.

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