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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

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, (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.

Containing 4 - (biphenyl ethynyl) - 1, 8 naphthalene imide liquid crystal compound, preparation method and application thereof

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Paragraph 0029; 0036; 0037; 0038, (2019/02/21)

The invention discloses a liquid crystal compound containing 4-(biphenyl acetenyl)-1,8 naphthalimide, a preparing method and application. Solubility of molecules in mixed liquid crystal is improved by the compound, the linear structure of the molecules is

Fluorescent dichroic dye containing 3-(biphenylethynyl) acenaphtho [1,2-b] quinoxaline, preparation method of fluorescent dichroic dye and application of fluorescent dichroic dye

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Paragraph 0039; 0040; 0041, (2017/05/13)

The invention discloses a fluorescent dichroic dye containing 3-(biphenylethynyl) acenaphtho [1,2-b] quinoxaline, a preparation method of the fluorescent dichroic dye and application of the fluorescent dichroic dye, and the type of fluorescent dichroic dye is enriched. The condensation of o-phenylenediamine on the biocarbonyl groups of acenaphthene broadens the conjugation system of a molecule, improves the rigidity and co-planarity of the molecule, and is beneficial to orientation in the main liquid crystal. The coupling of biphenyl acetylene groups to the biocarbonyl groups of the acenaphthene through a coupling reaction extends the conjugation linearity of the molecule. The fluorescent dichroic dye containing 3-(biphenylethynyl) acenaphtho [1,2-b] quinoxaline is novel in 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 introduction of different alkyl terminal chains in this type of fluorescent dichroic dye increases the solubility of the molecule in a liquid crystal, strengthens the linear structure of the molecule and improves the dichroism of the dye.

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