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15797-52-1

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15797-52-1 Usage

General Description

1,3,5-Tris(4-hydroxyphenyl)benzene 97 is a chemical compound with the molecular formula C21H18O3. It is a white, crystalline solid that is mainly used as an intermediate in the synthesis of organic compounds and polymers. 1 3 5-TRIS(4-HYDROXYPHENYL)BENZENE 97 is also known as phloroglucinol tris(4-hydroxyphenyl)benzene and is commonly used as a building block in the production of epoxy resins, flame retardants, and pharmaceuticals. It possesses antioxidant properties and is often used in the production of materials that require high heat resistance and durability, such as electrical insulating materials and adhesives. Additionally, 1,3,5-Tris(4-hydroxyphenyl)benzene 97 is considered to have low toxicity and low environmental impact, making it a desirable choice for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 15797-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,9 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15797-52:
(7*1)+(6*5)+(5*7)+(4*9)+(3*7)+(2*5)+(1*2)=141
141 % 10 = 1
So 15797-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H18O3/c25-22-7-1-16(2-8-22)19-13-20(17-3-9-23(26)10-4-17)15-21(14-19)18-5-11-24(27)12-6-18/h1-15,25-27H

15797-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3,5-bis(4-hydroxyphenyl)phenyl]phenol

1.2 Other means of identification

Product number -
Other names 1,3,5-TRIS(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:15797-52-1 SDS

15797-52-1Relevant articles and documents

Facile synthetic routes to phenylene and triazine core based dendritic cobaltabisdicarbollides

Dash, Barada Prasanna,Satapathy, Rashmirekha,Maguire, John A.,Hosmane, Narayan S.

, p. 5230 - 5235 (2010)

The synthesis and thermal properties of phenylene and triazine core based symmetrical macromolecules containing three to six cobaltabis(dicarbollide) clusters are reported. The zwitterionic oxonium derivative of cobaltabis(dicarbollide), [3,3′-Co(8-C4H8O 2-1,2-C2B9H10)(1′,2′- C2B9H11)], has been used for the synthetic transformations, and silicon tetrachloride and triflic acid were used as the cyclotrimerization reagents. Compounds containing multiple cobaltabis(dicarbollide) clusters are found to be extremely thermally stable, and only a 10-30% mass loss occurred up to 700 °C.

Novel electron-beam molecular resists with high resolution and high sensitivity for nanometer lithography

Kadota, Toshiaki,Kageyama, Hiroshi,Wakaya, Fujio,Gamo, Kenji,Shirota, Yasuhiko

, p. 706 - 707 (2004)

A novel class of chemically-amplified, electron-beam molecular resists for nanometer lithography were created. These molecular resists functioned as positive resists in the presence of an acid generator, exhibiting a high sensitivity of ≈2 μC cm-2/s

Hydroxyphenylbenzene derivatives as glass forming molecules for high resolution photoresists

Ober, Christopher K.,De Silva, Anuja

, p. 1903 - 1910 (2008)

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.

Single-Crystalline MFI Zeolite with Sheet-Like Mesopores Layered along the a Axis

Zhang, Yunjuan,Shen, Xuefeng,Gong, Zheng,Han, Lu,Sun, Huai,Che, Shunai

, p. 738 - 742 (2019)

Designing a templating strategy for directing mesopore growth along different crystallographic directions is essential for fabricating two- or three-dimensional single-crystalline mesoporous zeolites. However, so far, mesopores formed in MFI zeolites by soft templates have mostly been generated by disrupting growth along the b axis; generating mesopores by disrupting growth along the a axis is rare. Herein, a single-crystalline mesoporous MFI zeolite (SCMMZ) with sheet-like mesopores layered along the a and b axes was synthesized using a triply branched surfactant with diquaternary ammonium groups connected to 1,3,5-triphenylbenzene by a six- and eight-carbon alkyl chain (TPB-6 and 8). The sheet-like mesopores were embedded in the MFI framework and were retained even after calcination. Molecular mechanics calculations provided evidence of low binding energy configurations of the surfactant that directed the growth of straight and zigzag channels along the b and a axes, respectively. The formation of nanosheets was attributed to the geometric matching of the arrangement of the aromatic groups to the zeolite framework.

Design and synthesis of C3-symmetric molecules containing oxepine and benzofuran moieties via Metathesis

Gupta, Naveen Kumar,Kotha, Sambasivarao,Solanke, Balaji. U.

, (2021/07/17)

We report a new synthetic strategy to C3-symmetric star-shaped phenyl and triazine central cores bearing oxepine and benzofuran ring systems. In this regard, we have explored the application of metathetic strategy to construct C3-sym

COMPOSITION FOR FILM FORMATION, FILM, RESIST UNDERLAYER FILM-FORMING METHOD, PRODUCTION METHOD OF PATTERNED SUBSTRATE, AND COMPOUND

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Paragraph 0194, (2019/04/14)

The composition for film formation includes a compound including a group of the formula (1) and a solvent. In the formula (1), R1 to R4 each independently represent a hydrogen atom, a monovalent organic group having 1 to 20 carbon at

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