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CAS

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1071469-53-8

2,5-diphenyl-3-(3-trifluoromethylphenylseleno)-selenophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1071469-53-8 Structure

  • Basic information

    1. Product Name: 2,5-diphenyl-3-(3-trifluoromethylphenylseleno)-selenophene
    2. Synonyms: 2,5-diphenyl-3-(3-trifluoromethylphenylseleno)-selenophene
    3. CAS NO:1071469-53-8
    4. Molecular Formula:
    5. Molecular Weight: 506.287
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1071469-53-8.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: 2,5-diphenyl-3-(3-trifluoromethylphenylseleno)-selenophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-diphenyl-3-(3-trifluoromethylphenylseleno)-selenophene(1071469-53-8)
    11. EPA Substance Registry System: 2,5-diphenyl-3-(3-trifluoromethylphenylseleno)-selenophene(1071469-53-8)

  • 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: 1071469-53-8(Hazardous Substances Data)

1071469-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1071469-53-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,4,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1071469-53:
(9*1)+(8*0)+(7*7)+(6*1)+(5*4)+(4*6)+(3*9)+(2*5)+(1*3)=148
148 % 10 = 8
So 1071469-53-8 is a valid CAS Registry Number.

1071469-53-8Downstream Products

1071469-53-8Relevant articles and documents

Synthesis and antidepressant-like activity of selenophenes obtained via iron(iii)-PhSeSePh-mediated cyclization of Z-selenoenynes

Gai, Bibiana M.,Stein, Andre L.,Roehrs, Juliano A.,Bilheri, Filipe N.,Nogueira, Cristina W.,Zeni, Gilson

supporting information; experimental part, p. 798 - 807 (2012/02/05)

We present here the synthesis and antidepressant-like action of a series of 2,5-disubstituted-3-(organoseleno)-selenophenes prepared by a novel synthetic route, the FeCl3-diorganyl dichalcogenide-mediated intramolecular cyclization of (Z)-chalc

Copper iodide-catalyzed cyclization of (Z)-chalcogenoenynes

Stein, Andre L.,Alves, Diego,Da Rocha, Juliana T.,Nogueira, Cristina W.,Zeni, Gilson

scheme or table, p. 4983 - 4986 (2009/05/07)

(Chemical Equation Presented) We present here our results of the efficient copper-catalyzed cyclizations of chalcogenoenynes and establish a route to obtain 3-substituted chalcogenophenes in good to excellent yields. In addition, the obtained chalcogenophenes were readily transformed to more complex products using the palladium-catalyzed cross-coupling reactions with boronic acids to give Suzuki-type products in good yields.

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