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477587-89-6

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477587-89-6 Usage

Chemical Properties

Light yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 477587-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,5,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 477587-89:
(8*4)+(7*7)+(6*7)+(5*5)+(4*8)+(3*7)+(2*8)+(1*9)=226
226 % 10 = 6
So 477587-89-6 is a valid CAS Registry Number.

477587-89-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-4-(4-ethynylphenyl)benzene

1.2 Other means of identification

Product number -
Other names 4-Ethyl-4'-ethynyl-1,1'-biphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:477587-89-6 SDS

477587-89-6Downstream Products

477587-89-6Relevant articles and documents

Synthesis method of 4-alkyl biphenylacetylene

-

, (2021/06/13)

The invention discloses a synthesis method of 4-alkyl biphenyl acetylene. The synthesis method comprises the following steps: carrying out catalytic hydrogenation reaction on 4-alkyl diketone to obtain 4-alkyl biphenyl; then reacting the 4-alkyl biphenyl with halogen to obtain 4-halogen-4 '-alkyl biphenyl; and allowing 4-halo-4 '-alkyl biphenyl and an ethynylation reagent to be subjected to a coupling reaction to obtain a compound shown in a formula (IV) under the action of alkali. The method creatively adopts a palladium catalyst and lewis acid combined catalytic system to carry out deoxidation reaction on 4-alkyl diketone, and has good selectivity and high yield; in addition, hydrogen is used as a hydrogen source, a byproduct is only water, and the method is environment-friendly.

Ferrocenyl palladacycles derived from unsymmetrical pincer-type ligands: Evidence of Pd(0) nanoparticle generation during the Suzuki-Miyaura reaction and applications in the direct arylation of thiazoles and isoxazoles

Maji, Ankur,Singh, Anshu,Mohanty, Aurobinda,Maji, Pradip K.,Ghosh, Kaushik

supporting information, p. 17083 - 17096 (2019/11/26)

A new family of ferrocenyl-palladacycle complexes Pd(L1)Cl (Pd1) and Pd(L2)Cl (Pd2) were synthesized and characterized by UV-visible, IR, ESI-MS, and NMR spectral studies. The molecular structures of Pd1 and Pd2 were determined by X-ray crystallographic studies. Palladacycle catalyzed Suzuki-Miyaura cross-coupling reactions were investigated utilizing the derivatives of phenylboronic acids and substituted chlorobenzenes. Mechanistic investigation authenticated the generation of Pd(0) nanoparticles during the catalytic cycle and the nanoparticles were characterized by XPS, SEM and TEM analysis. Direct C-H arylation of thiazole and isoxazole derivatives employing these ferrocenyl-palladacycle complexes was examined. The reaction model for the arylation reaction implicating the in situ generation of Pd(0) nanoparticles was proposed.

Fluorescent dichroic dye containing 4-biphenyl acetylene acenaphtho[1,2-b]pyrazine-8,9-dinitrile, preparation method of fluorescent dichroic dye and application of fluorescent dichroic dye

-

, (2017/06/02)

The invention discloses a fluorescent dichroic dye containing 4-biphenyl acetylene acenaphtho[1,2-b]pyrazine-8,9-dinitrile, a preparation method of the fluorescent dichroic dye and application of the fluorescent dichroic dye. The 4-biphenyl acetylene acenaphtho[1,2-b]pyrazine-8,9-dinitrile is synthesized by using acenaphthequinone as a parent body and has novel structure, the raw materials are easy to obtain and the synthesis method is simple. The fluorescent dichroic dye having high fluorescent quantum production rate is obtained. The maximum emission wavelength of the dye is 563nm, the dye shows yellow fluorescence, and fluorescence quantum yield is high in a range of 0.43-0.51 to meet the practical application requirements. The dye V has a maximum red shift of 101 nm. The fluorescent dichroic dye has an excellent dichroic ratio and an ordered parameter in the liquid crystal E7. Absorption ordered parameter is 0.41-0.51, fluorescent ordered parameter is 0.34-0.39, and the fluorescent dichroic dye can thus be used for guest-host type liquid crystal display. Please see the specific structural formula in the description.

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