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4084-45-1

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4084-45-1 Usage

Uses

Used in Research and Development:
[1,1':4',1''-Terphenyl]-4,4''-diol is used as a research compound in the chemistry industry for various applications. Its specific and detailed uses are limited due to its highly specialized nature, but it plays a crucial role in the development of new chemical processes and products.
Used in Chemical Industry:
In the chemical industry, [1,1':4',1''-Terphenyl]-4,4''-diol is used as an intermediate or building block for the synthesis of more complex organic compounds. Its unique structure and properties make it valuable for creating new materials with specific characteristics.
Used in Environmental Studies:
Due to its potential for bioaccumulation and low solubility in water, [1,1':4',1''-Terphenyl]-4,4''-diol is used in environmental studies to understand the behavior of similar non-polar compounds in ecosystems. This knowledge helps in assessing the environmental impact of such compounds and developing strategies for their safe handling and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 4084-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4084-45:
(6*4)+(5*0)+(4*8)+(3*4)+(2*4)+(1*5)=81
81 % 10 = 1
So 4084-45-1 is a valid CAS Registry Number.

4084-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1':4',1''-Terphenyl-4,4''-diol

1.2 Other means of identification

Product number -
Other names 4,4'-dihydroxyterphenylene

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:4084-45-1 SDS

4084-45-1Downstream Products

4084-45-1Relevant articles and documents

Concomitant polymorphs of 2,2′,6,6′-tetramethyl-4,4′- terphenyldiol: The β-quinol network reproduced in a metastable polymorph

Aitipamula, Srinivasulu,Nangia, Ashwini

, p. 3159 - 3161 (2005)

The striking resemblance of the rhombohedral and monoclinic forms of the title molecule to β- and γ-quinol provides a crystal engineering approach to new polymorphic systems. The Royal Society of Chemistry 2005.

DIAMINE COMPOUND, POLYIMIDE PRECURSOR AND POLYIMIDE FILM PREPARED BY USING SAME

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Paragraph 0315; 0316; 0368; 0369, (2020/09/26)

The present invention discloses a novel diamine including benzene rings connected by functional groups on both sides of a p-terphenyl structure in which three benzene rings are connected, and having a structure in which the benzene rings are substituted with various substituents. In addition, the present invention can provide a polyimide film having improved physical properties by including the novel diamine as a polymerization component.COPYRIGHT KIPO 2021

Polymerizable mesogen compound having improved photoreactive efficiency and polymerizable liquid crystal compositions containing the same

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Paragraph 0084; 0085; 0090; 0091, (2016/12/26)

The present invention relates to a polymerizable mesogen compound having improved photo-reaction efficiency by introducing an alpha-thiomethyl acrylate group as a photo-reactive group, and to a polymerizable liquid crystal composition containing the same. The polymerizable mesogen compound of the present invention has improved photo-reaction efficiency at a relatively low energy state by introducing an alpha-thiomethyl acrylate group as a photo-reactive group, retains excellent solubility in a host liquid crystal due to an asymmetric structure thereof, and improves stability of the pretilt angle after photo-crosslinking, and thus can be useful as a polymerizable liquid crystal composition, particularly, a polymerizable liquid crystal composition for a polymer stabilization alignment type liquid crystal display.

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