84420-28-0

Upstream product

• 135-76-2 sodium 2-naphthol-6-sulfonate 
• 62-53-3 aniline 
• 580-13-2 2-bromonaphthalene 
• 103-84-4 Acetanilid 
• 591-50-4 iodobenzene 
• 936-36-7 2-Naphthylamine monoanion 
• 114536-36-6 potassium 2-naphthylamide 
• 36611-02-6 naphthalen-2-yl-phenyl-aminyl 
• 27067-31-8 N-phenyl 2-naphthyl nitroxide 
• 515-42-4 sodium phenylsulfonate 
• 91-59-8 naphthalen-2-ylamine 
• 91-20-3 naphthalene 
• 622-37-7 Phenyl azide 
• 3857-83-8 2-naphthyl triflate 

Downstream Products

• 74495-79-7 N-(2-naphthyl)-N-phenyl-acetamide 
• 4523-36-8 N-phenyl-1-(phenyldiazen-yl)naphthalen-2-amine 
• 55566-61-5 2-(2-anilino-[1]naphthylazo)-benzoic acid 
• 854458-72-3 2,3-bis-(4-methoxy-2-methyl-phenyl)-buta-1,3-diene 
• 38455-57-1 9-anilino-7-phenyl-benzo[a]phenazinium; chloride 
• 115605-51-1 1-hydroxy-[2]naphthoic acid-([2]naphthyl-phenyl-amide) 
• 116496-14-1 4-(2'-N-phenylaminonaphthylazo)toluene 
• 6364-05-2 N-methyl-N-phenylnaphthalen-2-amine 
• 17704-04-0 o-semidine 
• 412312-73-3 N-[2]naphthyl-N-phenyl-thiourea 
• 21784-66-7 2-anilinonaphthalene-8-sulfonic acid 
• 83662-03-7 6-anilino-naphthalene-1-sulfonic acid 
• 818-67-7 acrylic acid methallyl ester 

Relevant academic research and scientific papers

A quick Chan-Lam C-N and C-S cross coupling at room temperature in the presence of square pyramidal [Cu(DMAP)4I]I as a catalyst

A rapid and efficient protocol for C-N and C-S cross coupling has been developed using a new square pyramidal copper complex, [Cu(DMAP)4I]I. The complex was successfully synthesized via a disproportionation reaction of CuI and DMAP in DMSO. The catalytic activity of the complex was found to be excellent for Chan-Lam coupling reaction between aryl boronic acid and amine, amide, azide or thiol. The reaction could be carried out in the presence of only 2 mol% of the copper catalyst in methanol at room temperature within a short time.

Organic compound, electronic component, comprising same and electronic device

The invention provides an organic compound, an electronic component comprising the same and an electronic device, and belongs to the technical field of organic electroluminescence. The compound provided by the invention contains condensed rings of carbazole and fluorene, dibenzofuran or dibenzothiophene, has a rigid plane structure and high light-emitting quantum efficiency, and can improve the thermal stability and film stability of a material. According to the invention, the low triplet state energy level is effectively improved; and the compound is used for a light-emitting layer in a red light device, can effectively improve non-uniformity of charge transmission, improves the light-emitting efficiency and stability of the device, and effectively improves the performance of the device.

Organic compound, and electronic element and electronic device using same

The invention relates to an organic compound. The structure of the organic compound is shown as a formula I. When the organic compound is used as a hole adjustment layer material of an electronic element, driving voltage can be reduced, the luminous efficiency of a device can be improved, and the service life of the device can be prolonged.

Nitrogen-containing compound, organic electroluminescent device, and electronic device

The invention provides a nitrogen-containing compound, an organic electroluminescent device and an electronic device, and belongs to the technical field of organic materials. The structure of the nitrogen-containing compound is represented by Chemical Formula 1: wherein X1, X2, Y1, Y2 are the same or different from each other and are each independently a single bond, O, S, N(R3), C(R4R5), Ge(R6R7), Si(R8R9), Se, wherein X1 and Y1 are not single bonds simultaneously and X2 and Y2 are not single bonds simultaneously.

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 the luminous efficiency, stability, and lifespan of a device, an organic electric device using the same, and an electronic apparatus thereof. By using a compound according to the present invention, high luminous efficiency, low driving voltage, and high heat resistance of the device can be achieved, and color purity and lifespan of the device can be greatly improved.

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.

Triarylamine derivative and organic electroluminescent device thereof

The invention provides a triarylamine derivative and an organic electroluminescent device thereof, and relates to the technical field of organic electroluminescence. The triarylamine derivative provided by the invention has a higher triplet energy level. When the organic electroluminescent device is applied to the organic electroluminescent device, the driving voltage of the organic electroluminescent device can be effectively reduced, the luminous efficiency is improved, and the service life of the device is prolonged.

CO2-tuned highly selective reduction of formamides to the corresponding methylamines

We herein describe an efficient, CO2-tuned and highly selective C-O bond cleavage of N-methylated formanilides. With easy-to-handle and commercially available NaBH4 as the reductant, a variety of formanilides could be turned into the desired tertiary amines in moderate to excellent yields. The role of CO2 has been investigated in detail, and the mechanism is proposed on the basis of experiments.

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

The present invention relates to a novel compound, an organic electric element using the same, and an electronic device thereof. According to the present invention, a luminous efficiency, a color purity and a lifespan of the element can be improved and a driving voltage can be lowered. The organic electric element comprises: an anode; a cathode; and an organic material layer formed between the anode and the cathode.