73183-55-8

Usage

Chiral compound

Exists as a racemic mixture of enantiomers

Building block

Used in the synthesis of various pharmaceuticals and bioactive molecules

Pharmacological properties

Potential as a beta-adrenergic receptor agonist and use in the treatment of cardiovascular conditions

Organic synthesis

Versatile intermediate in the preparation of various organic compounds

Industry applications

Potential applications in both the pharmaceutical and organic synthesis industries

Upstream product

• 591-50-4 iodobenzene 
• 108-20-3 di-isopropyl ether 
• 35708-19-1 Methyl N-phenylanthranilate 
• 108-86-1 bromobenzene 
• 91-40-7 2-(phenylamino)benzoic acid 
• 676-58-4 methylmagnesium chloride 
• 23699-74-3 1-(2-anilinophenyl)ethan-1-one 
• 917-54-4 methyllithium 
• 62-53-3 aniline 
• 7073-69-0 2-(2-bromophenyl)propanol 
• 134-20-3 2-carbomethoxyaniline 
• 74-83-9 methyl bromide 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 1342892-15-2 10-(4-bromophenyl)-9,9-dimethyl-9,10-dihydro-acridine 
• 1643935-09-4 9,9-dimethyl-10-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9.10-dihydroacridine 
• 1628752-98-6 10-(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl) -9,9-dimethyl-9,10-dihydroacridine 
• 1314019-66-3 (9,9-dimethyl-10-phenyl-9,10-dihydroacridin-2-yl)boronic acid 
• 1443680-94-1 2-bromo-9,9-dimethyl-9,10-dihydroacridine 

Relevant academic research and scientific papers

Novel organic compounds for organic light-emitting diode and organic light-emitting diode including the same

The present invention relates to an organic light emitting compound represented by formula A and an organic light emitting diode including the same. Substituents A1 to A4, R1 to R17, X, Y, a, b, m, n, p, L1, and L2 are identical to as defined in the detailed description.

Carbazole derivatives and organoelectro luminescent device using the same

PURPOSE: A carbazole derivative is provided to drive an organic electroluminescent device at low voltage and to improve brightness when the derivative is used in an organic layer of the organic electroluminescent device, thereby improving economic efficiency. CONSTITUTION: A carbazole derivative is denoted by chemical formula 1. An organic electroluminescent device comprises a first electrode, a second electrode, and one or more organic layers between the first and second electrodes. The organic layers contain the carbazole derivative of chemical formula 1. The organic layers are selected among a hole injection layer, a hole transport layer, a functional layer with hole injecting and transporting functions, a light emitting layer, an electrode transport layer, and an electron injection layer. The light emitting layer contains one or more host compounds and one or more dopant compounds. The host compound is a carbazole derivative of chemical formula 1.

Deuterated organic compounds for organic light-emitting diode and organic light-emitting diode including the same

The present invention relates to an organic electroluminescent compound represented by chemical formula A and an organic light emitting device comprising the same. Substituents Y, Ar2 , L3 , K, p and x are as defined in the description of the invention. [Chemical A] (by machine translation)

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to an organic luminescent compound represented by chemical formula 1 and an organic electroluminescent device including the same. The organic luminescent compound according to the present invention has excellent luminous efficiency and lifetime properties of material, and thus, enables the manufacturing of an organic electroluminescent device having excellent luminous efficiency while having power efficiency and long lifetime properties. [Chemical formula 1].

Heterocyclic com pounds and organic light-emitting diode including the same

The present invention relates to a novel heterocyclic compound and an organic electroluminescent device comprising the same. The heterocyclic compound is represented by the following Chemical Formula 1, and the organic electroluminescent device including the heterocyclic compound has excellent driving voltage, luminous efficiency, and lifespan properties. Chemical Formula 1. (by machine translation)

Near-Infrared BODIPY-Acridine Dyads Acting as Heavy-Atom-Free Dual-Functioning Photosensitizers

Boron dipyrromethene (BODIPY) dyes represent a particular class within the broad array of potential photosensitizers. Their highly fluorescent nature opens the door for theragnostic applications, combining imaging and therapy using a single, easily synthesized chromophore. However, near-infrared absorption is strongly desired for photodynamic therapy to enhance tissue penetration. Furthermore, singlet oxygen should preferentially be generated without the incorporation of heavy atoms, as these often require additional synthetic efforts and/or afford dark cytotoxicity. Solutions for both problems are known, but have never been successfully combined in one simple BODIPY material. Here, we present a series of compact BODIPY-acridine dyads, active in the phototherapeutic window and showing balanced brightness and phototoxic power. Although the donor–acceptor design was envisioned to introduce a charge transfer state to assist in intersystem crossing, quantum-chemical calculations refute this. Further photophysical investigations suggest the presence of exciplex states and their involvement in singlet oxygen formation.

Photoelectric conversion element, imaging device, optical sensor, and method of using photoelectric conversion element

The present invention provides a photoelectric conversion element having a photoelectric conversion film which exhibits excellent photoelectric conversion efficiency and responsiveness, an imaging device, an optical sensor, and a method of using a photoelectric conversion element. In the photoelectric conversion element of the invention, a photoelectric conversion material contains at least one selected from the group consisting of a compound represented by General formula (1), a compound represented by General formula (2), and a compound represented by General formula (3).

Method for preparing 9,9-dimethyl acridine

The invention belongs to the technical field of organic synthesis and in particular relates to a method for preparing 9,9-dimethyl acridine. The method provided by the invention comprises the following steps: mixing 2-(2-(phenyl amino) phenyl) propane-2-alcohol and a hydrogen type molecular sieve based catalyst in an organic solvent, carrying out a reaction for 2-4 hours at 20-50 DEG C, carrying out solid-liquid separation so as to obtain a liquid phase, and removing the organic solvent in the liquid phase, so as to obtain the 9,9-dimethyl acridine. The method has the advantages of being gentle in reaction condition, simple and convenient in operation, green and environment-friendly and high in product yield and is applicable to large-scale industrial production and application, and the catalyst can be recycled and repeatedly used.

ORGANIC COMPOUND, AND ORGANIC LIGHT-EMITTING DIODE AND ORGANIC LIGHT-EMITTING DIODE DISPLAY DEVICE INCLUDING THE SAME

An organic compound is represented by the Formula below, and an organic light-emitting diode and an organic light-emitting diode display device include the organic compound.

A benzhydryl radical based on the room temperature of the organic light-emitting material and using the material preparation of organic electroluminescent device

A benzhydryl radical based on the stability of the organic light-emitting material at room temperature and using the material preparation of the organic electroluminescent device, which belongs to the field of organic light-emitting technology. The present invention in the preparation of the organic light-emitting material, the center of the common characteristic is the carbon free radical, is composed of two C - C covalent bond and a C - N to form a covalent bond. Stability is the light-emitting free radical material in the application of the key nature, connected to the electronic group conducive to stable free radical, in this invention through the nitrogen-containing heterocyclic carbazole, indole, dimethyl acridine and the like in the electronic group to the nitrogen atom is connected directly to the benzyl group, to obtain a stable benzhydryl radical, its stability and PTM, compared with the TTM is greatly improved, and has a room temperature fluorescent. The preparation of the material of the organic electroluminescent device using double thread condition exciton light-emitting, can avoid the traditional organic electroluminescent device in the use of the triplet state exciton, the maximum external quantum efficiency of the device is 0.66%.