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CAS

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1616667-76-5

2',3'-O-isopropylidene-8-(4-trifluoromethylphenyl)inosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1616667-76-5 Structure

  • Basic information

    1. Product Name: 2',3'-O-isopropylidene-8-(4-trifluoromethylphenyl)inosine
    2. Synonyms: 2',3'-O-isopropylidene-8-(4-trifluoromethylphenyl)inosine
    3. CAS NO:1616667-76-5
    4. Molecular Formula:
    5. Molecular Weight: 452.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1616667-76-5.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'-O-isopropylidene-8-(4-trifluoromethylphenyl)inosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2',3'-O-isopropylidene-8-(4-trifluoromethylphenyl)inosine(1616667-76-5)
    11. EPA Substance Registry System: 2',3'-O-isopropylidene-8-(4-trifluoromethylphenyl)inosine(1616667-76-5)

  • 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: 1616667-76-5(Hazardous Substances Data)

1616667-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1616667-76-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,6,6 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1616667-76:
(9*1)+(8*6)+(7*1)+(6*6)+(5*6)+(4*6)+(3*7)+(2*7)+(1*6)=195
195 % 10 = 5
So 1616667-76-5 is a valid CAS Registry Number.

1616667-76-5Relevant articles and documents

Microwave-assisted synthesis of C-8 aryl and heteroaryl inosines and determination of their inhibitory activities against Plasmodium falciparum purine nucleoside phosphorylase

Gigante, Alba,Priego, Eva-María,Sánchez-Carrasco, Paula,Ruiz-Pérez, Luis Miguel,Vande Voorde, Johan,Camarasa, María- José,Balzarini, Jan,González-Pacanowska, Dolores,Pérez-Pérez, María-Jesús

, p. 459 - 465 (2014)

8-Arylinosines have been scarcely studied for therapeutic purposes, probably due to difficulties in their synthesis. The recently described direct arylation reaction at position 8 of purine nucleosides has been employed to synthesize a series of 8-aryl and 8-pyridylinosines. These compounds have been studied for hydrolytic stability and subjected to biological evaluation. Three compounds have shown a pronounced specific inhibition of Plasmodium falciparum-encoded purine nucleoside phosphorylase, an important target for antimalarial chemotherapy.

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