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4-(pentyloxy)-3-(trifluoromethyl)benzenamine is a chemical compound with the molecular formula C13H15F3NO. It is an aniline derivative featuring a trifluoromethyl group and a pentyloxy group attached to a benzene ring. 4-(pentyloxy)-3-(trifluoromethyl)benzenamine is known for its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, and may serve as a building block in organic synthesis. Its properties could also make it suitable for specialized materials and coatings, although further research is required to explore its full potential.

832099-33-9

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832099-33-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(pentyloxy)-3-(trifluoromethyl)benzenamine is used as an intermediate in the synthesis of new drugs for various therapeutic applications. Its unique structure allows for the development of compounds with specific pharmacological properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical field, 4-(pentyloxy)-3-(trifluoromethyl)benzenamine is used as a precursor in the production of pesticides and other agrochemicals. Its chemical properties can be harnessed to create effective and targeted pest control solutions, enhancing crop protection and yield.
Used in Materials Science:
4-(pentyloxy)-3-(trifluoromethyl)benzenamine is utilized in materials science for the development of specialized materials and coatings. Its chemical structure may impart unique properties to these materials, such as improved stability, durability, or specific interactions with other substances, broadening its applications in various industries.
Used in Organic Synthesis:
As a building block in organic synthesis, 4-(pentyloxy)-3-(trifluoromethyl)benzenamine enables the creation of a wide range of organic compounds with diverse applications. Its presence in these syntheses can lead to the development of new molecules with potential uses in various sectors, including pharmaceuticals, agrochemicals, and materials science.
Further research and testing are necessary to fully understand the potential uses and properties of 4-(pentyloxy)-3-(trifluoromethyl)benzenamine, ensuring its safe and effective application in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 832099-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,0,9 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 832099-33:
(8*8)+(7*3)+(6*2)+(5*0)+(4*9)+(3*9)+(2*3)+(1*3)=169
169 % 10 = 9
So 832099-33-9 is a valid CAS Registry Number.

832099-33-9SDS

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-pentoxy-3-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 4-pentyloxy-3-trifluoromethylphenylamine

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:832099-33-9 SDS

832099-33-9Upstream product

832099-33-9Relevant academic research and scientific papers

Substituted aryl acylthioureas and related compounds; inhibitors of viral replication

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Page/Page column 32, (2008/06/13)

The invention provides compounds and pharmaceutically acceptable salts of Formula I wherein the variables A1, A2, R1, R2, V, W, X, Y, and Z are defined herein. Certain compounds of Formula I described herein whi

SUBSTITUTED ARYLTHIOUREA DERIVATIVES USEFUL AS INHIBITORS OF VIRAL REPLICATION

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Page/Page column 52, (2010/02/10)

Substituted arylthiourea compounds of Formula I, and the pharmaceutically acceptable salts of such compounds, useful as antiviral agents, are provided herein. Certain substituted arylthioureas disclosed herein are potent and/ or selective inhibitors of viral replication, particularly Hepatitis C virus replication. Pharmaceutical compositions containing one or more substituted arylthiourea compounds and one or more pharmaceutically acceptable carriers, excipients, or diluents are provided herein. Such pharmaceutical compositions may contain a substituted arylthiourea as the only active agent or may contain a combination of a substituted arylthiourea derivative and one or more other pharmaceutically active agents. Methods of treating Hepatitis C viral infections in mammals are also provided herein.

SUBSTITUTED ARYLACYLTHIOUREA, ITS RELATED COMPOUND, AND INHIBITOR OF VIRUS REPLICATION

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Page/Page column 99, (2008/06/13)

PROBLEM TO BE SOLVED: To provide an arylthiourea derivative and its related compound, useful as an antiviral agent. SOLUTION: This compound of formula I (A1, A2, R1, R2, V, W, X, Y and Z are each specifically de

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