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1,4-bis(biphenyl-2-yl)-2,5-difluorobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1380586-82-2

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1380586-82-2 Usage

Chemical structure

1,4-bis(biphenyl-2-yl)-2,5-difluorobenzene consists of a central benzene ring with two fluorine atoms at positions 2 and 5, and two biphenyl groups attached at position 1 and 4.

Family

It belongs to the family of fluoroarenes.

Applications

Often used as a building block in the synthesis of organic materials and pharmaceutical compounds.

Thermal stability

Exhibits excellent thermal stability, making it a valuable starting material for the production of high-performance polymers and liquid crystal materials.

Chemical stability

Also exhibits excellent chemical stability.

Molecular structure

Has a symmetrical molecular structure.

Fluorine substitution

The presence of fluorine atoms in the molecule makes it a useful molecule for studying molecular recognition and supramolecular chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1380586-82-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,8 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1380586-82:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*8)+(3*6)+(2*8)+(1*2)=182
182 % 10 = 2
So 1380586-82-2 is a valid CAS Registry Number.

1380586-82-2Downstream Products

1380586-82-2Relevant academic research and scientific papers

Intramolecular aryl-aryl coupling of fluoroarenes through Al 2O3-mediated HF elimination

Amsharov, K.Yu.,Merz

, p. 5445 - 5448 (2012)

A strategy for effective intramolecular aryl-aryl coupling of fluoroarenes through Al2O3-mediated HF elimination is reported. It is demonstrated that the C-F bond, which is widely believed to be the most passive functionality in organic chemistry, can be reconsidered as a useful functional group allowing very effective C-C bond formation. The solid-state strategy presented in this study opens the possibility for facile syntheses of insoluble extended polycyclic aromatic hydrocarbons.

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