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2,3,4,5,6-pentafluoro-1,1':4',1:4,1'''-quaterphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1129495-32-4 Structure
  • Basic information

    1. Product Name: 2,3,4,5,6-pentafluoro-1,1':4',1:4,1'''-quaterphenyl
    2. Synonyms: 2,3,4,5,6-pentafluoro-1,1':4',1:4,1'''-quaterphenyl
    3. CAS NO:1129495-32-4
    4. Molecular Formula:
    5. Molecular Weight: 396.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1129495-32-4.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: 2,3,4,5,6-pentafluoro-1,1':4',1:4,1'''-quaterphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,5,6-pentafluoro-1,1':4',1:4,1'''-quaterphenyl(1129495-32-4)
    11. EPA Substance Registry System: 2,3,4,5,6-pentafluoro-1,1':4',1:4,1'''-quaterphenyl(1129495-32-4)
  • 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: 1129495-32-4(Hazardous Substances Data)

1129495-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1129495-32-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,9,4,9 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1129495-32:
(9*1)+(8*1)+(7*2)+(6*9)+(5*4)+(4*9)+(3*5)+(2*3)+(1*2)=164
164 % 10 = 4
So 1129495-32-4 is a valid CAS Registry Number.

1129495-32-4Downstream Products

1129495-32-4Relevant articles and documents

One-pot synthesis of polyfluoroterphenyls via palladium-catalyzed Suzuki-Miyaura coupling of chlorobromobenzene and C-H bond functionalization of perfluoroarenes

Ma, Xiaowei,Gu, Ningning,Liu, Yan,Liu, Ping,Xie, Jianwei,Dai, Bin,Liu, Zhiyong

, p. 50 - 56 (2015)

An efficient tandem route for the synthesis of polyfluoroterphenyl derivatives has been developed. The target compounds were obtained in moderate to good yields by a Pd(OAc)2-catalyzed three-component coupling reaction involving palladium-catal

Palladium-Catalyzed Solid-State Polyfluoroarylation of Aryl Halides Using Mechanochemistry

Takahashi, Rikuro,Seo, Tamae,Kubota, Koji,Ito, Hajime

, p. 14803 - 14810 (2021/12/09)

The Suzuki–Miyaura cross-coupling between polyfluorinated arylboron nucleophiles and aryl halides enables the efficient construction of polyfluorinated structural motifs frequently found in organic materials and catalysts. A key challenge associated with

Palladium-catalyzed direct arylation of polyfluoroarene and facile synthesis of liquid crystal compounds

Ma, Xiaowei,Liu, Yan,Liu, Ping,Xie, Jianwei,Dai, Bin,Liu, Zhiyong

, p. 180 - 185 (2014/03/21)

A convenient approach has been developed to prepare polyfluorobiphenyl by Pd(OAc)2/PCy3-catalyzed direct arylation of polyfluoroarenes with aromatic halides in the presence of Cs2CO 3 as base and toluene as solvent. In most cases, the desired arylated products of aromatic bromides were obtained in good to excellent yield at 80°C, and aryl chlorides also gave modest to good yields of arylated products at 110°C. According to this efficient C - C bondforming method, polyfluorobiphenyl liquid crystal compounds were prepared by Pd-catalyzed direct arylation reactions of polyfluoroarenes with long alkyl chain substituted aryl bromides in 62-96% yield. Copyright

Synthesis of functionalized oligophenylenes and oligoarylenes bearing heteroaryl groups

Wallmann, Ivonne,Schnakenburg, Gregor,Luetzen, Arne

experimental part, p. 79 - 84 (2009/06/17)

Oligo-P-phenylenes have proven to be versatile building blocks for the generation of self-assembled nanoaggregates via vapour deposition on solid supports whose optical properties and morphologies can be influenced by the introduction of functional groups

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