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CAS

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1447730-02-0

2-(2,3,5-trifluoro-4-(trifluoromethyl)phenyl)quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1447730-02-0 Structure

  • Basic information

    1. Product Name: 2-(2,3,5-trifluoro-4-(trifluoromethyl)phenyl)quinoline
    2. Synonyms: 2-(2,3,5-trifluoro-4-(trifluoromethyl)phenyl)quinoline
    3. CAS NO:1447730-02-0
    4. Molecular Formula:
    5. Molecular Weight: 327.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1447730-02-0.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: 2-(2,3,5-trifluoro-4-(trifluoromethyl)phenyl)quinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,3,5-trifluoro-4-(trifluoromethyl)phenyl)quinoline(1447730-02-0)
    11. EPA Substance Registry System: 2-(2,3,5-trifluoro-4-(trifluoromethyl)phenyl)quinoline(1447730-02-0)

  • 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: 1447730-02-0(Hazardous Substances Data)

1447730-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1447730-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,7,3 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1447730-02:
(9*1)+(8*4)+(7*4)+(6*7)+(5*7)+(4*3)+(3*0)+(2*0)+(1*2)=160
160 % 10 = 0
So 1447730-02-0 is a valid CAS Registry Number.

1447730-02-0Relevant articles and documents

Palladium-catalyzed ortho-selective c-f activation of polyfluoroarenes with triethylsilane: A facile access to partially fluorinated aromatics

Chen, Zhao,He, Chun-Yang,Yin, Zengsheng,Chen, Liye,He, Yi,Zhang, Xingang

, p. 5813 - 5817 (2013)

PdF: A simple catalytic system, broad substrate scope, and high versatility provide a useful and facile access to partially fluorinated aromatics (see scheme). Tuning the reaction conditions enables a diverse range of product structures to be prepared. Copyright

Fluorine-containing aromatic derivatives of selective hydrogenation reduction method

-

Paragraph 0191; 0192; 0193; 0194; 0262, (2017/11/27)

The invention discloses a selective hydrogenation reduction method of a fluorine-containing aromatic hydrocarbon derivative, and particularly discloses a preparation method of a compound shown in a general formula C1, C2 or C3. The preparation method comprises the following step of: reacting a compound shown in a general formula A1, A2 or A3 with a compound shown in a general formula B in the presence of a catalyst, thus forming the compound shown in the general formula C1, C2 or C3.

Nickel-catalyzed ortho-selective hydrodefluorination of N-containing heterocycle-polyfluoroarenes

He, Yi,Chen, Zhao,He, Chun-Yang,Zhang, Xingang

, p. 873 - 877 (2013/08/23)

An effective and facile method for preparation of partially fluorinated aromatics via Nickel catalyzed, chelation-assisted ortho selective hydrodefluorination of polyfluoroarnes with triethylsilane has been developed, in which N-containing heterocycles were used as directing groups. The advantage of this protocol is its simple catalytic system with use of inexpensive and readily available NiCl2·6H2O as a catalyst. An effective and facile method for preparation of partially fluorinated aromatics via Nickel catalyzed, chelation-assisted ortho selective hydrodefluorination of polyfluoroarnes with triethylsilane has been developed, in which N-containing heterocycles were used as directing groups. Copyright

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