37529-30-9

Usage

Uses

Used in Chemical Synthesis:
4-N-DECYLANILINE is used as a key intermediate in the synthesis of various organic compounds, particularly in the production of p,p'-Di-n-decyl-azobenzol. 4-N-DECYLANILINE is obtained through a reaction involving 4-Decylaniline, oxygen (O2), copper(II) chloride (CuCl), and pyridine as reagents. The resulting p,p'-Di-n-decyl-azobenzol has potential applications in the field of materials science, particularly in the development of novel materials with specific optical, electronic, or magnetic properties.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 4-N-DECYLANILINE, due to its amine functional group and hydrophobic decyl chain, could potentially be used in the pharmaceutical industry for the development of new drugs or drug delivery systems. Its amphiphilic nature may allow it to act as a surfactant or stabilizer in the formulation of drug delivery systems, enhancing the solubility and bioavailability of poorly water-soluble drugs.
Used in Dye and Pigment Industry:
Given its structural similarity to aniline, 4-N-DECYLANILINE could be used in the synthesis of dyes and pigments, particularly those requiring a hydrophobic component. The decyl chain in 4-N-DECYLANILINE may impart unique solubility properties to the resulting dyes or pigments, making them suitable for specific applications in the textile, plastics, or printing industries.
Used in Polymer Industry:
The hydrophobic nature of the decyl group in 4-N-DECYLANILINE may also make it a candidate for use in the polymer industry, where it could be used as a comonomer in the synthesis of polymers with tailored properties. These polymers could have applications in various fields, such as coatings, adhesives, or membranes, where specific surface or interfacial properties are desired.

InChI:InChI=1/C16H27N/c1-2-3-4-5-6-7-8-9-10-15-11-13-16(17)14-12-15/h11-14H,2-10,17H2,1H3

Upstream product

• 112-30-1 1-Decanol 
• 62-53-3 aniline 
• 71-43-2 benzene 
• 1423616-68-5 4-(dec-1-yn-1-yl)aniline 
• 764-93-2 1-decyne 
• 540-37-4 p-aminoiodobenzene 
• 6048-82-4 decanophenone 
• 104-72-3 decylbenzene 
• 153195-09-6 (E)-1-(dec-1-enyl)-4-nitrobenzene 
• 103-84-4 Acetanilid 
• 112-13-0 n-decanoyl chloride 
• 101888-18-0 acetic acid-(4-decanoyl-anilide) 
• 142-04-1 aniline hydrochloride 
• 101449-24-5 4'-aminodecanoylphenone 

Downstream Products

• 37593-13-8 N-(4-decylphenyl)acetamide 
• 37593-00-3 p,p'-Di-n-decyl-azobenzol 
• 315716-39-3 4-Decyl-2-iodoaniline 
• 620180-53-2 4-((4-decylphenyl)diazenyl)phenol 
• 448959-69-1 [2-benzyloxy-1-(4-decyl-phenylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester 
• 68777-59-3 [1-Biphenyl-4-yl-meth-(Z)-ylidene]-(4-decyl-phenyl)-amine 
• 1306630-54-5 C₅₂H₆₁N₅O₆ 
• 1423617-06-4 4-bromo-2-(4-decylphenyl)-7-methoxyisoindoline-1,3-dione 
• 1423617-08-6 2-(4-decylphenyl)-4-methoxy-7-((trimethylsilyl)ethynyl)isoindoline-1,3-dione 
• 1423616-72-1 5-bromo-2-(4-decylphenyl)isoindoline-1,3-dione 
• 1493763-08-8 1-azido-4-decylbenzene 

Relevant academic research and scientific papers

CLASS II HMG-COA REDUCTASE INHIBITORS AND METHODS OF USE

Disclosed are compositions and methods for treating bacterial infections.

Nickel-catalyzed decarbonylative polymerization of 5-alkynylphthalimides: A new methodology for the preparation of polyheterocycles

A nickel-catalyzed decarbonylative cycloaddition was developed, in which 5-alkynylphthalimides reacted to afford a new type of polyisoquinolone. It was demonstrated for the first time that decarbonylative cycloaddition can be an elementary process of polycondensation for the preparation of heterocyclic polymers.

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.

Therapeutic agent for osteoporosis and diazepine compound

A therapeutic agent for osteoporosis, comprising an azepine compound of the formula STR1 wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof as an active ingredient, a method for treating osteoporosis comprising administering said compound and a use of said compound for the production of a therapeutic agent for osteoporosis. The compounds of the formula (I) have superior bone resorption-inhibitory activity and act to reduce the increased amount of calcium in blood serum, which is caused by bone resorption. Accordingly, these compounds are usable as pharmaceutical agents to effectively inhibit bone resorption, to prevent decrease of bone mass and to prevent or suppress the increase of calcium amount in blood serum which is caused by the progress of bone resorption, with regard to Paget's disease, hypercalcemia, osteoporosis and so on in which the progress of bone resorption is considered to be deeply associated with the symptom, and to the symptoms of progressing bone resorption (development into osteoporosis) along with inflammatory joint diseases such as rheumatoid arthritis.

Liquid crystal compounds and optically active compounds

A compound usefull for liquid crystal component which is represented by the following formulas (1), (2), (3), or (4) ;, R1 -X1 -A1 -( A2 )n-Y1 -A3 -X2 -R2 (1), R1 -X1 -( A3 -Y1 )N-A1 -A2 -X2 -R2 (2), R3 -X1 -A4 -Y1 -A3 -X2 -R4 (3), R3 -X1 -A5 -Y1 -A1 -A2 -X2 -R4 (4), wherein R1 ,R2 ,R3 and R4 are C1 18 alkyl groups; X1 and X2 is -, O, S, -C≡C- or divarent groups such as COO, OCO, CH2 O or OCH2

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.

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.