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3-[3-(3-aminophenoxy)propoxy]aniline is a chemical compound that belongs to the group of diphenyl ethers, which are aromatic compounds with two benzene rings connected through an ether group. Its systematic name is [(3-aminophenyl)oxy]propoxybenzene. 3-[3-(3-aminophenoxy)propoxy]aniline is characterized by a benzene ring substituted with an amine group and an oxygen atom linked to a propoxybenzene moiety. Its molecular structure features interconnected rings, including cyclised hydrocarbon rings and a nitrogen atom. The specific structure of 3-[3-(3-aminophenoxy)propoxy]aniline endows it with certain chemical properties, such as increased reactivity in specific types of chemical reactions. It is utilized in various processes, particularly in the pharmaceutical and chemical industries. As with many chemicals, it is essential to exercise caution when handling 3-[3-(3-aminophenoxy)propoxy]aniline to mitigate potential health risks.

6245-49-4

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6245-49-4 Usage

Uses

Used in Pharmaceutical Industry:
3-[3-(3-aminophenoxy)propoxy]aniline is used as an intermediate or active ingredient for the synthesis of various pharmaceutical compounds. Its unique molecular structure allows it to be a key component in the development of drugs with specific therapeutic properties.
Used in Chemical Industry:
3-[3-(3-aminophenoxy)propoxy]aniline is employed as a reagent or catalyst in chemical reactions, particularly those that require its heightened reactivity. Its presence can facilitate the synthesis of complex molecules or improve the efficiency of certain chemical processes.
Used in Research and Development:
3-[3-(3-aminophenoxy)propoxy]aniline is utilized as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure makes it an interesting subject for scientific investigation, which could lead to new discoveries and applications in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 6245-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6245-49:
(6*6)+(5*2)+(4*4)+(3*5)+(2*4)+(1*9)=94
94 % 10 = 4
So 6245-49-4 is a valid CAS Registry Number.

6245-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[3-(3-aminophenoxy)propoxy]aniline

1.2 Other means of identification

Product number -
Other names 3,3'-Propandiyldioxy-di-anilin

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:6245-49-4 SDS

6245-49-4Downstream Products

6245-49-4Relevant academic research and scientific papers

Potent and selective double-headed thiophene-2-carboximidamide inhibitors of neuronal nitric oxide synthase for the treatment of melanoma

Huang, He,Li, Huiying,Yang, Sun,Chreifi, Georges,Martásek, Pavel,Roman, Linda J.,Meyskens, Frank L.,Poulos, Thomas L.,Silverman, Richard B.

, p. 686 - 700 (2014/03/21)

Selective inhibitors of neuronal nitric oxide synthase (nNOS) are regarded as valuable and powerful agents with therapeutic potential for the treatment of chronic neurodegenerative pathologies and human melanoma. Here, we describe a novel hybrid strategy

Thiophene-2-carboximidamide Based Selective Neuronal Nitric Oxide Inhibitors

-

Paragraph 0030, (2014/03/25)

Selective neuronal nitric oxide synthase (nNOS) inhibitor compounds designed with one or more thiophene-2-carboximidamide substituents for improved bioavailability.

Guanidine compound and heat sensitive recording material

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Page column 35, (2010/01/30)

An object of the present invention is to provide a heat sensitive recording material which can develop color at high density by the inclusion of a novel guanidine compound which is strongly basic and superior in diffusion resistance. The present invention for attaining the above-described object is a heat sensitive recording material comprising a substrate supporting thereon a heat sensitive recording layer containing a diazonium salt compound, a coupler which reacts with the diazonium salt compound when heated to develop color, and abase, wherein the heat sensitive recording layer includes as the base at least one of the guanidine compounds represented by the general formula (1): wherein, in the general formula (1), R1and R2represent an alkyl group or aryl group and may be the same or different, R3and R4represent a hydrogen atom, alkyl group or halogen atom and may be the same or different, and X represents a divalent connecting group.

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