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137529-56-7

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137529-56-7 Usage

Description

1,2,3-trifluoro-5-4-[2-(4-pentylcyclohexyl)ethyl]cyclohexylbenzene is a complex organic chemical compound characterized by a benzene ring with three fluorine atoms at the 1, 2, and 3 positions. It features a 5-substituted group that includes a cyclohexyl and a pentyl group, with the cyclohexyl group further substituted by an ethyl group. This intricate molecular structure, with its fluorine atoms and multiple alkyl groups, suggests potential applications in various fields due to its unique physical and chemical properties.

Uses

Used in Organic Synthesis:
1,2,3-trifluoro-5-4-[2-(4-pentylcyclohexyl)ethyl]cyclohexylbenzene is used as a building block in organic synthesis for the creation of more complex molecules. Its fluorinated benzene ring and diverse alkyl groups provide a versatile platform for further chemical reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, or specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,2,3-trifluoro-5-4-[2-(4-pentylcyclohexyl)ethyl]cyclohexylbenzene is used as a potential active pharmaceutical ingredient (API) or as a key intermediate in the synthesis of APIs. Its unique structure may offer specific biological activities or serve as a prodrug that can be metabolized into an active form within the body, contributing to the development of new therapeutic agents.
Used in Material Science:
1,2,3-trifluoro-5-4-[2-(4-pentylcyclohexyl)ethyl]cyclohexylbenzene is used in material science for the development of new materials with tailored properties. The presence of fluorine atoms and the complex arrangement of the molecule may endow it with specific characteristics such as enhanced stability, solubility, or reactivity, making it suitable for applications in coatings, polymers, or advanced materials.
Used in Chemical Research:
In the field of chemical research, 1,2,3-trifluoro-5-4-[2-(4-pentylcyclohexyl)ethyl]cyclohexylbenzene serves as a subject of study to explore its physical and chemical properties. Understanding its reactivity, stability, and interactions with other molecules can provide insights into new reaction mechanisms, catalysis, or the development of novel synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 137529-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,5,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 137529-56:
(8*1)+(7*3)+(6*7)+(5*5)+(4*2)+(3*9)+(2*5)+(1*6)=147
147 % 10 = 7
So 137529-56-7 is a valid CAS Registry Number.

137529-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-Trifluoro-5-{4-[2-(4-pentylcyclohexyl)ethyl]cyclohexyl}benz ene

1.2 Other means of identification

Product number -
Other names -

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

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More Details:137529-56-7 SDS

137529-56-7Downstream Products

137529-56-7Relevant articles and documents

Trifluorinated liquid crystals for TFT displays

Demus,Goto,Sawada,Nakagawa,Saito

, p. 1 - 21 (2007/10/02)

3, 4, 5-tri-fluorobenzene derivatives with different core structures have been synthesized and their physical properties have been determined. Most of the compounds are nematic with broad existence regions. The materials have large dielectric anisotropy, low viscosity, low optical anisotropy and very good voltage holding ratio and high chemical stability and are valuable components for mixtures to be used in TFT displays. The good voltage holding ratio of the compounds is related to their high electrical resistivity. In order to reproduce the dependence of the resistivity on the dielectric constant, we derived a general formula. Its derivation is based on the interaction of the impurity ions with the induced and permanent dipoles of the liquid crystal molecules. We are able to show, that ion/ion interactions in highly purified liquid crystals may be neglected.

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