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1,4-diethynyl-2-fluorobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137000-66-9

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137000-66-9 Usage

Molecular structure

A benzene ring with two fluorine atoms at the 1 and 4 positions, and two ethynyl groups at the 2 position.

Derivative

Benzene

Family

Diethynylbenzene

Applications

Organic synthesis, materials science, liquid crystals, organic semiconductors, chemical sensors, and as a building block for novel organic compounds.

Reactivity

High due to the presence of multiple triple bonds.

Physical state

Likely a solid or liquid at room temperature (not specified in the material).

Stability

Not specified in the material.

Solubility

Not specified in the material.

Melting point

Not specified in the material.

Boiling point

Not specified in the material.

Density

Not specified in the material.

Appearance

Not specified in the material.

Odor

Not specified in the material.

Safety

Not specified in the material, but caution should be taken when handling due to its reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 137000-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,0 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 137000-66:
(8*1)+(7*3)+(6*7)+(5*0)+(4*0)+(3*0)+(2*6)+(1*6)=89
89 % 10 = 9
So 137000-66-9 is a valid CAS Registry Number.

137000-66-9Upstream product

137000-66-9Relevant academic research and scientific papers

Fluorinated porous organic frameworks for improved CO2 and CH4 capture

Comotti,Castiglioni,Bracco,Perego,Pedrini,Negroni,Sozzani

, p. 8999 - 9002 (2019)

A porous 3D selectively fluorinated framework (F-PAF1), robust yet flexible and with a surface area of 2050 m2 g-1, was synthesised by condensation of an ad hoc prepared fluorinated tetraphenylmethane (TPM) monomer to ensure homogenously distributed C-F dipoles in the swellable architecture. Tetradentate TPM was also the comonomer for the reaction with fluorinated difunctional monomers to obtain frameworks (FMFs) with a controlled amount of regularly spaced reorientable C-F dipoles. The isosteric heat of adsorption of CO2 was increased by 53% by even moderate C-F dipole insertion, with respect to the non-fluorinated frameworks. CO2/N2 selectivity was also increased up to a value of 50 for the difluoro-containing comonomer. Moreover, methane shows optimal interaction energies of 24 kJ mol-1.

Steps to demarcate the effects of chromophore aggregation and planarization in poly(phenyleneethynylene)s. 2. The photophysics of 1,4-diethynyl-2-fluorobenzene in solution and in crystals

Levitus,Zepeda,Dang,Godinez,Khuong,Schmieder,Garcia-Garibay

, p. 3188 - 3195 (2001)

Crystals of 1,4-bis(2-hydroxy-2-methyl-3-butynyl)-2-fluorobenzene 4 have a rich packing structure with four distinct molecules in the unit cell. A complex hydrogen bonding network results in the formation of cofacial trimers, cofacial dimers, and monomers

Polymerizable compound having conjugated bonds, liquid crystal composition and liquid crystal display device

-

Page/Page column 74; 75; 76, (2019/04/26)

Subject It is to provide a polymerizable compound having a high polymerization reactivity, a high conversion yield and a high solubility in a liquid crystal composition, a polymerizable composition including this compound, a liquid crystal composite prepared from this polymerizable composition and a liquid crystal display device containing this composite. Means for solving the Subject A compound represented by formula (1), the liquid crystal composition and the liquid crystal display device. In the formula, for example, ring A1, ring A2 and ring A4 are phenylene or cyclohexylene; Sp1 and Sp2 are a single bond or alkylene having 1 to 6 carbons; Z1 and Z2 are —CH═CH— or —C≡C—; a is 1, b is 0; and P1 and P2 are a polymerizable group.

A versatile approach to β-amyloid fibril-binding compounds exploiting the shirakawa/hayashi protocol for trans-alkene synthesis

Huynh, Tri H. V.,Mantel, Mette Louise H.,Mikkelsen, Katrine,Lindhardt, Anders T.,Nielsen, Niels ChR.,Otzen, Daniel,Skrydstrup, Troels

supporting information; experimental part, p. 999 - 1002 (2009/07/18)

Application of the Sonogashira coupling reaction followed by a trans-selective alkyne reduction proved highly adaptable for the efficient synthesis of a class of β-amyloid fibril binding compounds possessing a styrylbenzene motif such as FSB, an FSB dimer

Synthesis and optical characterisation of platinum(II) poly-yne polymers incorporating substituted 1,4-diethynylbenzene derivatives and an investigation of the intermolecular interactions in the diethynylbenzene molecular precursors

Khan, Muhammad S.,Al-Mandhary, Muna R. A.,Al-Suti, Mohammed K.,Corcoran, Timothy C.,Al-Mahrooqi, Yaqoub,Attfield, J. Paul,Feeder, Neil,David, William I. F.,Shankland, Kenneth,Friend, Richard H.,Koehler, Anna,Marseglia, Elisabeth A.,Tedesco, Emilio,Tang, Chiu C.,Raithby, Paul R.,Collings, Jonathan C.,Roscoe, Karl P.,Batsanov, Andrei S.,Stimson, Lorna M.,Marder, Todd B.

, p. 140 - 149 (2007/10/03)

A series of 1,4-diethynylbenzene (1) derivatives, H-C≡C-R-C≡C-H with R = C6H3NH2 (2), C6H3F (3), C6H2F2-2,5 (4), C6F4 (5), C6H2/

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