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ethyl 2,3,4-tri-O-acetyl-S-(N-tosylimino)-1-thio-α-L-rhamnopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 406947-00-0 Structure
  • Basic information

    1. Product Name: ethyl 2,3,4-tri-O-acetyl-S-(N-tosylimino)-1-thio-α-L-rhamnopyranoside
    2. Synonyms: ethyl 2,3,4-tri-O-acetyl-S-(N-tosylimino)-1-thio-α-L-rhamnopyranoside
    3. CAS NO:406947-00-0
    4. Molecular Formula:
    5. Molecular Weight: 503.595
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 406947-00-0.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: ethyl 2,3,4-tri-O-acetyl-S-(N-tosylimino)-1-thio-α-L-rhamnopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2,3,4-tri-O-acetyl-S-(N-tosylimino)-1-thio-α-L-rhamnopyranoside(406947-00-0)
    11. EPA Substance Registry System: ethyl 2,3,4-tri-O-acetyl-S-(N-tosylimino)-1-thio-α-L-rhamnopyranoside(406947-00-0)
  • 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: 406947-00-0(Hazardous Substances Data)

406947-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406947-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,9,4 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 406947-00:
(8*4)+(7*0)+(6*6)+(5*9)+(4*4)+(3*7)+(2*0)+(1*0)=150
150 % 10 = 0
So 406947-00-0 is a valid CAS Registry Number.

406947-00-0Relevant articles and documents

Synthesis of anomeric sulfimides and their use as a new family of glycosyl donors

Chery, Florence,Cassel, Stephanie,Wessel, Hans Peter,Rollin, Patrick

, p. 171 - 180 (2002)

We introduce a convenient synthesis of anomeric sulfimides, the ability of which to act as glycosyl donors has been tested with various thiophilic reagents and acceptors.

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