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CAS

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57577-40-9

2,3-dihydro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indole-2,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57577-40-9 Structure

  • Basic information

    1. Product Name: 2,3-dihydro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indole-2,3-dione
    2. Synonyms: 2,3-dihydro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indole-2,3-dione
    3. CAS NO:57577-40-9
    4. Molecular Formula:
    5. Molecular Weight: 591.574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57577-40-9.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: 2,3-dihydro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indole-2,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-dihydro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indole-2,3-dione(57577-40-9)
    11. EPA Substance Registry System: 2,3-dihydro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indole-2,3-dione(57577-40-9)

  • 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: 57577-40-9(Hazardous Substances Data)

57577-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57577-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57577-40:
(7*5)+(6*7)+(5*5)+(4*7)+(3*7)+(2*4)+(1*0)=159
159 % 10 = 9
So 57577-40-9 is a valid CAS Registry Number.

57577-40-9Downstream Products

57577-40-9Relevant articles and documents

Synthesis and antiviral evaluation of isatin ribonucleosides

De Oliveira, Mara R. P.,Torres, Jose C.,Garden, Simon J.,Dos Santos, Carla Veronica B.,Rocha Alves, Thatyana,Pinto, Angelo C.,Pereira, Helena de S.,Leao Ferreira, Luiz Roberto,Moussatche, Nissin,Frugulhetti, Izabel Christina de P. P.,Ferreira, Vitor F.,De Souza, Maria Cecilia B. V.

, p. 825 - 835 (2002)

A series of novel substituted isatin ribonucleosides 3b-3f were synthesized in good yields by a TMSOTf catalysed coupling reaction between the silylated nitrogenated base (1b-1f) and 1-O-acetyl-2,3,5-tri- O-benzoyl-β-D-ribofuranose (2). Isatin nucleoside 3a previously reported was also prepared using this method giving high yield. From the compounds tested, ribonucleoside 3f proved to be the most active one when assayed for antiviral activitiy on HSV-1 infected cells, leading to 66% of inhibition of virus yield. All the isatin derivatives tested did not inhibit HIV-1 Reverse Transcriptase (RT) activity.

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