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1333241-01-2

C22H11F3N2O11 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1333241-01-2 Structure

  • Basic information

    1. Product Name: C22H11F3N2O11
    2. Synonyms: C22H11F3N2O11
    3. CAS NO:1333241-01-2
    4. Molecular Formula:
    5. Molecular Weight: 536.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333241-01-2.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: C22H11F3N2O11(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H11F3N2O11(1333241-01-2)
    11. EPA Substance Registry System: C22H11F3N2O11(1333241-01-2)

  • 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: 1333241-01-2(Hazardous Substances Data)

1333241-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333241-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333241-01:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*4)+(3*1)+(2*0)+(1*1)=102
102 % 10 = 2
So 1333241-01-2 is a valid CAS Registry Number.

1333241-01-2Downstream Products

1333241-01-2Relevant articles and documents

Antifungal activity of a novel quercetin derivative bearing a trifluoromethyl group on Candida albicans

Tempesti, Tomas C.,Alvarez, M. Gabriela,Durantini, Edgardo N.,De Araujo, Marcelo Francisco,Catunda Jr., Francisco Eduardo Aragao,De Carvalho, Mario Geraldo

, p. 2217 - 2222,6 (2012)

In this study, a novel quercetin derivative bearing a trifluoromethyl group was synthesized by the nucleophilic aromatic substitution reaction between rutin and 2-chloro-5-(trifluoromethyl)-1,3-dinitrobenzene in basic medium. This synthetic quercetin showed antifungal activity against Candida albicans cultures. The results indicated a remarkable increase in the biological activity of this compound as compared to rutin.

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