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4-[2-(pyridin-4-yl)ethyl]aniline is an organic compound with the molecular formula C15H16N2. It is a derivative of aniline, featuring a pyridine ring attached to the ethyl group, which in turn is connected to the aniline moiety. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. Its structure provides a unique combination of aromatic and heterocyclic characteristics, which can influence its reactivity and physical properties. The compound is typically synthesized through chemical reactions involving aniline and pyridine derivatives, and its properties are of interest to researchers in the field of organic chemistry and drug development.

6318-70-3

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6318-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6318-70-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6318-70:
(6*6)+(5*3)+(4*1)+(3*8)+(2*7)+(1*0)=93
93 % 10 = 3
So 6318-70-3 is a valid CAS Registry Number.

6318-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-pyridin-4-ylethyl)aniline

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6318-70-3 SDS

6318-70-3Relevant academic research and scientific papers

Second-generation aryl isonitrile compounds targeting multidrug-resistant Staphylococcus aureus

Kyei-Baffour, Kwaku,Mohammad, Haroon,Seleem, Mohamed N.,Dai, Mingji

, p. 1845 - 1854 (2019/03/28)

Antibiotic resistance remains a major global public health threat that requires sustained discovery of novel antibacterial agents with unexploited scaffolds. Structure-activity relationship of the first-generation aryl isonitrile compounds we synthesized led to an initial lead molecule that informed the synthesis of a second-generation of aryl isonitriles. From this new series of 20 compounds, three analogues inhibited growth of methicillin-resistant Staphylococcus aureus (MRSA) (from 1 to 4 μM) and were safe to human keratinocytes. Compound 19, with an additional isonitrile group exhibited improved activity against MRSA compared to the first-generation lead compound. This compound emerged as a candidate worthy of further investigation and further reinforced the importance of the isonitrile functionality in the compounds’ anti-MRSA activity. In a murine skin wound model, 19 significantly reduced the burden of MRSA, similar to the antibiotic fusidic acid. In summary, 19 was identified as a new lead aryl isonitrile compound effective against MRSA.

Rho-kinase inhibitors

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

Disclosed are compounds and derivatives thereof, their synthesis, and their use as Rho-kinase inhibitors. These compounds are useful for inhibiting tumor growth, treating erectile dysfunction, and treating other indications mediated by Rho-kinase, e.g., c

Troger's base molecular scaffolds in dicarboxylic acid recognition

Goswami, Shyamaprosad,Ghosh, Kumaresh,Dasgupta, Swagata

, p. 1907 - 1914 (2007/10/03)

Artificial receptors (1-5) have been designed and synthesized from simple precursors. The chain length selectivity studies of dicarboxylic acids within the cavities of new fluorescent Troger's base molecular frameworks (1- 3) have been carried out with a critical examination of their role of rigidity as well as flexibility in selective binding in comparison to receptor 5. The chiral resolution of the racemic Troger's base receptors (1 and 2) by chiral recognition with (+)- camphoric acid using hydrogen-bonding interactions has been studied.

Studies on antiulcer drugs. V. Synthesis and antiulcer activity of aralkylbenzazoles

Katsura,Inoue,Tomoi,Takasugi

, p. 2062 - 2074 (2007/10/02)

A series of 2-alkylamino-5- or 6-aralkyl-substituted benzazoles were synthesized and tested for histamine H2-receptor antagonist and anti-stress ulcer activities. These new compounds showed little or no histamine H2-receptor antagoni

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