6314-38-1

Usage

Uses

Used in Pharmaceutical Industry:
(4-METHOXY-PHENYL)-NAPHTHALEN-1-YL-AMINE is used as a building block for the synthesis of pharmaceuticals. Its unique chemical structure allows it to be a valuable component in the development of new drugs, potentially contributing to the treatment of various medical conditions.
Used in Dye Industry:
In the dye industry, (4-METHOXY-PHENYL)-NAPHTHALEN-1-YL-AMINE is used as a building block for the synthesis of dyes. Its chemical properties make it suitable for creating a wide range of colors and shades, expanding the possibilities for dye manufacturers.
Used in Agrochemical Industry:
(4-METHOXY-PHENYL)-NAPHTHALEN-1-YL-AMINE is also used as a building block in the synthesis of agrochemicals. Its potential applications in this industry include the development of new pesticides, herbicides, and other agricultural products to improve crop yield and protect plants from pests.
Used in Organic Synthesis:
As an intermediate in organic synthesis, (4-METHOXY-PHENYL)-NAPHTHALEN-1-YL-AMINE plays a crucial role in the production of various chemical compounds. Its versatility in chemical reactions makes it a valuable asset in the synthesis of a wide range of products.
Used in Chemical Research:
(4-METHOXY-PHENYL)-NAPHTHALEN-1-YL-AMINE is used as a reagent in chemical research. Its unique properties and potential biological and pharmacological activities make it an interesting subject for further exploration and study in the fields of medicine and drug discovery.

InChI:InChI=1/C17H15NO/c1-19-15-11-9-14(10-12-15)18-17-8-4-6-13-5-2-3-7-16(13)17/h2-12,18H,1H3

Upstream product

• 134-32-7 1-amino-naphthalene 
• 104-94-9 4-methoxy-aniline 
• 90-13-1 1-Chloronaphthalene 
• 90-11-9 1-Bromonaphthalene 
• 86-53-3 1-Cyanonaphthalene 
• 879-18-5 naphthalene-1-carbonic acid chloride 
• 64300-03-4 N-(3,4-dihydro-1(2H)-naphthalenylidene)-4-methoxybenzenamine 
• 90-14-2 1-Iodonaphthalene 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 68211-49-4 1-naphthyl tosylate 
• 90-15-3 α-naphthol 

Downstream Products

• 1211403-56-3 C₂₆H₂₃NO₃ 
• 1211403-57-4 C₂₃H₁₇NO₂ 
• 1211403-58-5 C₄₁H₂₇N₃O 
• 1211403-59-6 C₄₈H₃₉N₃O₃ 
• 1211403-60-9 C₄₆H₃₅N₃O₃ 
• 1211403-63-2 C₅₀H₃₈N₄O₅ 
• 1392275-97-6 N-dichloromethyl-N-(4-methoxyphenyl)-N-(1-naphthyl)amine 
• 1392275-91-0 N-(4-methoxyphenyl)-N-(1-naphthyl)formamide 
• 6949-70-8 diethyl-[2-(9-methoxy-benzo[a]phenothiazin-12-yl)-ethyl]-amine 
• 879505-49-4 N,N'-bis(4-methoxyphenyl)-(1,1'-binaphthyl)-4,4'-diamine 
• 86538-44-5 9-hydroxy-7-methylbenzacridine 

Relevant academic research and scientific papers

Nickel-Catalyzed Amination of Aryl Nitriles for Accessing Diarylamines through C?CN Bond Activation

A nickel-catalyzed amination to access diarylamines has been developed through C?CN bond activation of aryl nitriles with anilines. In this developed catalytic protocol, various aromatic and heteroaromatic nitriles could be utilized as the electrophiles to couple with substituted anilines. A diversity of diarylamines were obtained in 15–95% yields. (Figure presented.).

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

In the present invention, provided is a novel compound capable of improving luminance efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof. By using the compound of the present invention, high luminance efficiency, low driving voltages, and high heat resistance of the element can be achieved, and color purity and service life of the element can be greatly improved.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

The present invention provides a novel compound capable of improving light emitting efficiency, stability, and lifespan of an element, an organic electronic element using same, and an electronic device for the same. In one aspect, the present invention provides a compound represented by the following chemical formula 1. The compounds according to the present invention by utilizing a light emitting device of high efficiency, low driving voltage, high heat resistance can be achieved, and the color purity of the device can greatly improve the service life.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

The present invention provides a novel compound capable of improving luminance efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof. By using the compound of the present invention, high luminance efficiency, low driving voltage, and high heat resistance of the element can be achieved, and color purity and service life of the element can be greatly improved.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

Discloses a novel compound capable of improving the luminous efficiency, stability and lifetime of an element, and an organic electronic element, or an electronic device using the same. (by machine translation)

COMPOUND FOR AN ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

The present invention provides a novel compound capable of improving light emitting efficiency, stability, and lifespan of an element, an organic electronic element using same, and an electronic device for the same. In one aspect, the present invention provides a compound represented by combination of chemical formula 1 and chemical formula 2. The compounds according to the present invention by utilizing a light emitting device of high efficiency, low driving voltage, high heat resistance can be achieved, and the color purity of the device can greatly improve the service life.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

PURPOSE: A compound containing bisindole for an organic electronic element is provided to improve light emitting efficiency, heat resistance, color purity, and lifetime and to lower driving voltage. CONSTITUTION: A compound for an organic electronic element contains compounds of chemical formulas 1 and 2. The organic electronic element contains one or more organic layers containing the compound. The organic layers are formed of the compounds by a solution process. The organic electronic element sequentially comprises a first electrode, the organic layers, and a second electrode. The organic layers are selected among a light emitting layer, a hole injection layer, a hole transport layer, an electron injection layer, and an electron transport layer. An electronic device comprises a display device containing the organic electronic element, and a control unit which drives the display device.

Organic compound with tetrahedral-like geometry

An organic compound with a tetrahedral-like geometry is disclosed. The organic compound has a structure represented by formula (I): wherein A1 to A4 each independently represent a 5-membered or 6-membered unsaturated ring; B1 represents direct bonding, —C—, —O—, —N—, —S— or —C═C—; m is 0 or 1; each of Ra's is independently hydrogen, fluorine, oxygen, substituted or unsubstituted C1-C12 alkyl or substituted or unsubstituted C6-C12 aryl; and n is an integer of 0 to 2.

Organic compound having tetrahedron-like configuration

The present invention relates to an organic compound having a tetrahedron-like configuration, wherein the organic compound has a structure represented by the following general formula (I) defined in the specification, A1-A4 are respectively and independently an unsaturated five-membered ring or an unsaturated six-membered ring, B is a direct bond , -C, -O-, -N-, -S-, or -C=C-, m is 0 or 1, Ris hydrogen, fluorine, substituted or unsubstituted C1-C12 alkyl, or substituted or unsubstituted C6-C12 aryl, and n is an integer of 0-2. The organic compound of the present invention has excellentphotoelectric property.

Nickel Dual Photoredox Catalysis for the Synthesis of Aryl Amines

In this work, a new dual photoredox nickel catalysis system has been utilized for the synthesize of aryl amines. Previously, our group has shown that a nickel catalyst in conjunction with a photosensitizer and a sacrificial electron donor can cross-couple C-C bonds via photoredox-assisted reductive coupling. Here we have built upon that system to develop a redox-neutral cross-coupling system for the formation of C-N bonds. The catalytic system is composed of just a nickel cross-coupling catalyst, a Ru photocatalyst, and base and is capable of coupling amines with aryl halides in good to excellent yields. Furthermore, it was found that these reactions are functional under ambient conditions with catalyst loadings of 1 mol %. Spectroscopic studies provide support that this amination mechanism proceeds via a nitrogen-based radical intermediate. This N-radical mechanism offers direct synthetic access to di- and triaryl amines from nickel photocatalysis.