2961-47-9

Usage

Uses

Used in Pharmaceutical Industry:
4-(5-Nonyl)pyridine is utilized as a key intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs. Its unique structure allows for the creation of molecules with specific therapeutic properties, enhancing the industry's capacity to address various health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(5-Nonyl)pyridine is employed as a precursor in the production of pesticides and other crop protection agents. Its incorporation into these products can improve their effectiveness in managing pests and diseases, thereby supporting agricultural productivity.
Used in Material Science:
4-(5-Nonyl)pyridine is explored for its potential use in the development of new materials such as polymers and surfactants. Its distinctive chemical structure offers opportunities for designing materials with tailored properties, useful in a range of applications from coatings to detergents.
Used in Research and Development:
4-(5-Nonyl)pyridine also serves as a valuable compound in research settings, where it is studied for its chemical properties and potential applications. Scientists and chemists use it to investigate new reactions and mechanisms, contributing to the broader understanding of organic chemistry and its practical applications.

InChI:InChI=1/C14H23N/c1-3-5-7-13(8-6-4-2)14-9-11-15-12-10-14/h9-13H,3-8H2,1-2H3

Upstream product

• 108-89-4 picoline 
• 109-65-9 1-bromo-butane 
• 290-37-9 1,4-pyrazine 
• 773837-37-9 sodium cyanide 
• 6277-35-6 N-methylpyrazinium iodide 

Downstream Products

• 72230-93-4 4,4'-di-(5-nonyl)-2,2'-bipyridine 
• 1126489-27-7 1-(5-(((3R,5S)-1,5-bis((benzyloxy)carbonyl)pyrrolidin-3-yl)oxy)-5-oxopentyl)-4-(1-butylpentyl)pyridinium bromide 
• 1126489-59-5 benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-serinate bromide 
• 1126489-60-8 benzyl N-((benzyloxy)carbonyl)-O-(5-(4-(1-butylpentyl)pyridinium-1-yl)pentanoyl)-L-threoninate bromide 

Relevant academic research and scientific papers

BIS-PYRIDINIUM COMPOUNDS

A method of treating, inhibiting, or preventing an infection in a subject is described. The method comprises administering to the subject an effective amount of at least one bis-pyridinium compound. The bis-pyridinium compound comprises two aromatic ring structures. Each of the ring structures comprises a pyridine ring, and the ring structures are linked by a linker group of at least 8 atoms in length, said linker group being attached to the nitrogen atoms of the pyridine rings. At least one substituent on at least one of the ring structures is an alkyl group having at least 2 carbon atoms, and no substituent on either of the ring structures is -OH, -SH or an amine group.

Pentacyanoferrates(II): Solvatochromism and Reactivity in Micelles and in Reversed Micelles

Rate constants for dissociation of pyridine derivatives from pentacyanoferrates(II), (3-), in micelles and in reversed micelles reflect significant interactions between the leaving ligands and the micelle or the water in the interior of the

Substituted 2,2'-bipyridyl compounds and process for preparing same

A process for preparing substituted 2,2'-bipyridyl compounds and several compounds so prepared, the process comprising the steps of first selecting a substituted pyridine of the formula defined herein, then mixing a stoichiometric excess of the substituted pyridine with an amount of sodamide, causing the resultant mixture to be at a temperature sufficiently high to cause substituted 2,2'-bipyridyl formation, and isolating the substituted 2,2'-bipyridyl thereby formed. The new substituted 2,2'-bipyridyl compounds are selected from the group consisting of 4,4'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(cyclohexylmethyl)-2,2'-bipyridyl; 5,5'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-phenylpropyl)-2,2'-bipyridyl; 4,4'-di-(4-tetrahydropyranyl)-2,2'-bipyridyl; 4,4'-di-benzyl-2,2'-bipyridyl; 6,6'-di-isoamyl-2,2'-bipyridyl; and 4,4'-di-(t-butyl)-2,2'-bipyridyl.