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3',4',5',6'-Tetrakis(4-hydroxyphenyl)-[1,1':2',1''-terphenyl]-4,4''-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

256495-17-7

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256495-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 256495-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,4,9 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 256495-17:
(8*2)+(7*5)+(6*6)+(5*4)+(4*9)+(3*5)+(2*1)+(1*7)=167
167 % 10 = 7
So 256495-17-7 is a valid CAS Registry Number.

256495-17-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2,3,4,5,6-pentakis(4-hydroxyphenyl)phenyl]phenol

1.2 Other means of identification

Product number -
Other names Hexakis(4-hydroxyphenyl)benzene

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:256495-17-7 SDS

256495-17-7Downstream Products

256495-17-7Relevant academic research and scientific papers

NOVEL COMPOUND, SEMICONDUCTOR MATERIAL, AND METHODS FOR MANUFACTURING COATING AND SEMICONDUCTOR USING THE SAME

-

Paragraph 0178; 0190; 0191, (2018/08/29)

PROBLEM TO BE SOLVED: To provide a semiconductor material and a coating having high solubility in solvents and having high filling property, high heat resistance, and/or high etching resistance, and to provide a method for manufacturing a semiconductor using the semiconductor material, and to provide a novel compound. SOLUTION: Provided are: a semiconductor material consisting of a specific aromatic hydrocarbon ring derivative; methods for manufacturing a coating and a semiconductor using the semiconductor material; and a compound consisting of a specific aromatic hydrocarbon ring derivative. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

NOVEL COMPOUND, SEMICONDUCTOR MATERIAL, AND METHODS FOR MANUFACTURING COATING AND SEMICONDUCTOR USING THE SAME

-

Paragraph 0061; 0065, (2018/07/29)

An object is to provide a semiconductor material and coating having high solubility in solvents and having advantageous filling property, high heat resistance, and/or high etching resistance. Another object is to provide a method for manufacturing a semiconductor using the semiconductor material. Still another object is to provide a novel compound. Provided are: a semiconductor material consisting of a specific aromatic hydrocarbon ring derivative; methods for manufacturing a coating and a semiconductor using the semiconductor material; and a compound consisting of a specific aromatic hydrocarbon ring derivative.

Hexaphenylbenzene as a rigid template for the straightforward syntheses of "star-shaped" glycodendrimers

Chabre, Yoann M.,Brisebois, Patrick P.,Abbassi, Leila,Kerr, Sheena C.,Fahy, John V.,Marcotte, Isabelle,Roy, Rene

, p. 724 - 727 (2011/03/22)

Original glycodendrimers emanating from propargylated hexaphenylbenzene cores and containing up to 54 peripheral sugar ligands have been synthesized by Cu(I)-catalyzed [1,3]-dipolar cycloadditions using both convergent and divergent approaches.

Hexameric subphthalocyanine rosette

Morisue, Mitsuhiko,Suzuki, Wataru,Kuroda, Yasuhisa

, p. 10047 - 10054 (2011/12/02)

A highly congested hexameric subphthalocyanine array was synthesized by axial chlorine-to-phenoxy substitution of a hexakis(4-hydroxyphenyl)benzene based subphthalocyanine, and photoinduced symmetry-breaking charge separation was demonstrated in polar solvent. The Royal Society of Chemistry 2011.

Hydroxyphenylbenzene derivatives as glass forming molecules for high resolution photoresists

Ober, Christopher K.,De Silva, Anuja

experimental part, p. 1903 - 1910 (2009/09/24)

This paper presents a fundamental study to relate molecular architecture to the amorphous properties of hydroxyphenylbenzene molecular glass derivatives. These studies demonstrates that the branched hydroxyphenylbenzene derivatives can form stable molecular glasses despite the π-π interactions present. Through this research, design concepts to stabilize the amorphous nature and to increase the glass transition temperature (Tg) based on asymmetric molecular structures, bulky substituents, conformation states and molecular size are explored. An understanding of such behavior is important for the development of hydroxyphenylbenzene derivatives as potential molecular photoresists for patterning below 50 nm. This research has helped to identify potential candidates to be evaluated as positive-tone photoresists for lithographic applications for extreme ultraviolet (EUV, λ = 13.4 nm) lithography. The first reported sub-30 nm feature sizes for hydroxyphenylbenzene derivatives were demonstrated with high Tg materials. The Royal Society of Chemistry.

Self-assembly of a radially functionalized hexagonal molecule: Hexakis(4-hydroxyphenyl)benzene

Kobayashi, Kenji,Shirasaka, Toshiaki,Sato, Azumi,Horn, Ernst,Furukawa, Naomichi

, p. 3483 - 3486 (2007/10/03)

Two different porous hydrogen-bonded networks are formed by self- assembly of the radially substituted host 1. In the network of type A, formed by 1 · 4Et2O, all OH groups of 1 are involved in hydrogen bonding, and the molecular sheets are stacked without translation to generate extended channels that accommodate the Et2O molecules. Four OH groups of 1 are involved in the type B network of 1 · 4DMF, and lateral translation of the sheets in an ABAB sequence generates large chambers, each of which contains four DMF molecules.

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