37529-29-6

Usage

Uses

Used in Chemical Industry:
P-N-Nonylaniline is used as an intermediate in the manufacturing of dyes and other chemical compounds for its ability to contribute to the formation of various colorants and chemical products.
Used in Research and Development:
P-N-Nonylaniline may be utilized in research and development settings to explore its properties and potential applications in various chemical processes, despite its hazardous nature.

InChI:InChI=1/C15H25N/c1-2-3-4-5-6-7-8-9-14-10-12-15(16)13-11-14/h10-13H,2-9,16H2,1H3

Upstream product

• 17763-80-3 para-nitrophenyl triflate 
• 3088-78-6 dihydroxy-nonyl-borane 
• 71-43-2 benzene 
• 6008-36-2 1-phenylnonan-1-one 
• 1081-77-2 n-nonylbenzene 
• 764-85-2 Nonanoyl chloride 
• 124-11-8 non-1-ene 
• 62-53-3 aniline 
• 143-08-8 nonyl alcohol 
• 80504-85-4 1-(4-nitrophenyl)-1,3-nonadiene 

Downstream Products

• 126332-10-3 [1-(4-Butoxy-phenyl)-meth-(E)-ylidene]-(4-nonyl-phenyl)-amine 
• 1306630-52-3 C₅₀H₅₇N₅O₆ 
• 80155-20-0 4-(4-Nonyl-phenylazo)-phenol 
• 1356840-19-1 4-n-nonylbenzeneboronic acid pinacolate 
• 1359844-16-8 C₁₅H₂₃I 
• 256383-45-6 (4-n-nonylphenyl)boronic acid 
• 1349697-55-7 C₄₇H₆₂N₂O₂S₂ 
• 132329-35-2 4-Octyloxy-benzoic acid 3-hydroxy-4-{[(E)-4-nonyl-phenylimino]-methyl}-phenyl ester 
• 132329-29-4 4-Heptyloxy-benzoic acid 3-hydroxy-4-{[(E)-4-nonyl-phenylimino]-methyl}-phenyl ester 
• 106132-85-8 (4-Nonyl-phenyl)-(4-propyl-phenyl)-diazene 
• 97586-30-6 5-Ethoxy-2-{[(E)-4-nonyl-phenylimino]-methyl}-phenol 

Relevant academic research and scientific papers

Design and synthesis of boronic acid inhibitors of endothelial lipase

Endothelial lipase (EL) and lipoprotein lipase (LPL) are homologous lipases that act on plasma lipoproteins. EL is predominantly a phospholipase and appears to be a key regulator of plasma HDL-C. LPL is mainly a triglyceride lipase regulating (V)LDL levels. The existing biological data indicate that inhibitors selective for EL over LPL should have anti-atherogenic activity, mainly through increasing plasma HDL-C levels. We report here the synthesis of alkyl, aryl, or acyl-substituted phenylboronic acids that inhibit EL. Many of the inhibitors evaluated proved to be nearly equally potent against both EL and LPL, but several exhibited moderate to good selectivity for EL.

Liquid-crystalline polymorphism of symmetrical azobananas: Bis(4-(4-alkylphenyl)azophenyl) 2-nitroisophtalates

In this paper we present a series of novel compounds, bis(4-(4-alkylphenyl) azophenyl) 2-nitroisophtalates, which exhibit nematic and banana-type liquidcrystalline phases. The alkyl chain length varies from 1 to 18 carbons. The first ten members of this series exhibit nematic phase. The last eleven compounds exhibit banana-type liquid crystalline phases. The propyl and pentyl derivatives have extra second type of banana mesophase. Copyright Taylor & Francis Group, LLC.

Ring alkylation of aniline or an aniline derivative using ionic liquid catalysts

A process for ring-alkylating aniline or an aniline derivative in which aniline or an aniline derivative is reacted with an alkylating agent in the presence of an ionic liquid which includes a Lewis acid and a quaternary cation, to produce a ring-alkylated alkylaniline or a ring-alkylated aniline derivative. The use of an ionic liquid permits convenient separation of the alkylated reaction product from the reactants.

Method for preparing aromatic secondary amino compound

Disclosed are (1) a method for preparing an aromatic secondary amino compound which comprises reacting an N-cyclohexylideneamino compound in the presence of a hydrogen moving catalyst and a hydrogen acceptor by the use of a sulfur-free polar solvent and/or a cocatalyst, and (2) a method for preparing an aromatic secondary amino compound which comprises reacting cyclohexanone or a nucleus-substituted cyclohexanone, an amine and a nitro compound corresponding to the amine in a sulfur-free polar solvent in the presence of a hydrogen moving catalyst, a cocatalyst being added or not added. In a further aspect, a method is provided for the preparation of aminodiphenylamine by reacting phenylenediamine and cyclohexanone in the presence of a hydrogen transfer catalyst in a sulfur-free polar solvent while using nitroaniline as a hydrogen acceptor.

Method for preparing aromatic secondary amino compound

Disclosed are (1) a method for preparing an aromatic secondary amino compound which comprises reacting an N-cyclohexylideneamino compound in the presence of a hydrogen moving catalyst and a hydrogen acceptor by the use of a sulfur-free polar solvent and/or a cocatalyst, and (2) a method for preparing an aromatic secondary amino compound which comprises reacting cyclohexanone or a nucleus-substituted cyclohexanone, an amine and a nitro compound corresponding to the amine in a sulfur-free polar solvent in the presence of a hydrogen moving catalyst, a cocatalyst being added or not added.

LIQUID CRYSTALLINE PROPERTIES OF 4-CHLOROBENZYLIDENE-4-AKYLANILINES

A new group of Schiff bases containing a polar terminal group was synthesized: .The alkyl was changed from n=1 to n=12.Based on calorimetric (DSC) studies and on observations of textures the phase situation was characterized.

METAL COMPLEXES IN ORGANIC SYNTHESIS. VIII. ALLYLIC ALCOHOLS AS STARTING MATERIALS IN PALLADIUM-CATALYZED WITTIG-TYPE OLEFINIZATIONS.

Allylic alcohols, aldehydes, and triphenylphosphine participate in a one-pot process catalyzed by palladium, which is formally equivalent to the Wittig olefinization. It can be applied to both aliphatic and aromatic aldehydes. The resulting olefins which appear as mixtures of stereoisomers were fully hydrogenated. Two different mechanisms can account for the observed results.

DOUBLE BOND FORMATION BY ONE POT PALLADIUM INDUCED REACTIONS BETWEEN ALDEHYDES, ALLYLIC ALCOHOLS AND TRIPHENYLPHOSPHINE

The reaction between several aldehydes, two allylic alcohols and triphenylphosphine under palladium catalysis leads to double bond formation, synthetically parallelizing the Wittig reaction.

Study of the Influence of Molecular Length on the Characteristics of the Ordered Smectic Phase.

Study of DTA and X-rays of p-phenyl-benzylidene-p'-alkylanilines of mesomorphic phases demonstrates the predominant role of the aliphatic chain length. In effect, it governs the appearance of the different phases; the correlation between layers decreases for greater chain lengths. The nonlinear variations of SmB layer thickness for these compounds shows clearly the importance of steric effects coupled with the molecular length with respect to the dipolar effect.