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1,1':3',1''-Terphenyl, 2',2''''-(1,2-ethynediyl)bis[4,4''-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

602277-55-4

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602277-55-4 Usage

Chemical structure

A terphenyl core with two ethynyl groups at the 2' and 2'' positions, and two 4,4''-dimethyl substituents.

Molecular weight

394.53 g/mol

Appearance

Colorless to pale yellow crystalline solid

Solubility

Insoluble in water, soluble in organic solvents such as ethanol, acetone, and toluene

Melting point

215-220°C

Boiling point

>400°C

Density

1.03 g/cm3

Refractive index

1.62

Symmetry

Highly symmetrical and rigid molecule

Applications

Polymer additive, component in liquid crystals, fluorescent material in OLEDs, potential applications in organic electronics and photovoltaics.

Note

The specific content provided in the material is limited, and some of the properties listed above are general properties of the compound based on its chemical structure and known properties of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 602277-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,2,2,7 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 602277-55:
(8*6)+(7*0)+(6*2)+(5*2)+(4*7)+(3*7)+(2*5)+(1*5)=134
134 % 10 = 4
So 602277-55-4 is a valid CAS Registry Number.

602277-55-4Downstream Products

602277-55-4Relevant academic research and scientific papers

Rotational isomerism involving an acetylenic carbon IV: synthesis and structure of bis(1,1';3',1"-terphenyl-2'-yl)ethynes: molecular design of sterically congested alkynes toward restricted rotation about acetylenic axis.

Toyota, Shinji,Iida, Taku,Kunizane, Chinatsu,Tanifuji, Naoki,Yoshida, Yukihiro

, p. 2298 - 2302 (2007/10/03)

The title diphenylethyne derivative with 4-methylphenyl (tolyl) groups at all the ortho positions was synthesized by the Stille or Sonogashira coupling from the corresponding iodide. The X-ray structure revealed that the two terminal phenyl groups at the

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