2915-16-4

Usage

Chemical Properties

white solid

InChI:InChI=1/C16H11ClN2/c17-16-18-14(12-7-3-1-4-8-12)11-15(19-16)13-9-5-2-6-10-13/h1-11H

Upstream product

• 3764-01-0 2,4,6-trichloropyrimidine 
• 98-80-6 phenylboronic acid 
• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 100-52-7 benzaldehyde 
• 98-86-2 acetophenone 
• 26032-72-4 2,4-dichloro-6-phenyl-pyrimidine 
• 40230-24-8 2-amino-4,6-diphenylpyrimidine 
• 108-86-1 bromobenzene 
• 120-46-7 1,3-diphenylpropanedione 
• 4120-05-2 2-hydroxy-4,6-diphenylpyrimidine 
• 4120-05-2 4,6-diphenyl-1H-pyrimidin-2-one 

Downstream Products

• 81668-39-5 (4,6-Diphenyl-pyrimidin-2-yl)-propyl-amine 
• 81668-40-8 N-butyl-4,6-diphenylpyrimidin-2-amine 
• 81668-41-9 (4,6-Diphenyl-pyrimidin-2-yl)-methyl-phenyl-amine 
• 88236-11-7 2-azido-4,6-diphenylpyrimidine 
• 135587-61-0 4,4',6,6'-tetraphenyl-2,2'-bipyrimidine 
• 106119-61-3 2-Hydroxyamino-4,6-diphenylpyrimidine 
• 4120-05-2 4,6-diphenyl-1H-pyrimidin-2-one 
• 81668-42-0 N-(4,6-Diphenyl-pyrimidin-2-yl)-N-ethyl-4-methyl-benzamide 
• 81668-43-1 N-(4,6-Diphenyl-pyrimidin-2-yl)-4-methyl-N-propyl-benzamide 
• 81668-44-2 N-Butyl-N-(4,6-diphenyl-pyrimidin-2-yl)-4-methyl-benzamide 
• 2915-23-3 4-(4,6-diphenyl-pyrimidin-2-yl)-benzene-1,3-diol 
• 1260249-11-3 6-(4,6-Diphenylpyrimidin-2-yl)-12,12-dimethyl-6,12-dihydro-6-azaindeno[1,2-b]fluorene 
• 1312205-95-0 C₅₅H₃₇N₅ 
• 1312205-92-7 C₅₅H₃₇N₅ 

Relevant academic research and scientific papers

Utilizing triazine/pyrimidine acceptor and carbazole-triphenylamine donor based bipolar novel host materials for highly luminescent green phosphorescent OLEDs with lower efficiency roll-off

In this work, two novel bipolar host materials were designed, synthesized and applied in green phosphorescent based OLEDs. Both the host materials, 4-(2-(4,6-diphenyl-1,3,5-triazin-2-yl)-9H-carbazol-9-yl)-N,N-diphenylaniline (TRZ 1) and 4-(2-(4,6-diphenylpyrimidin-2-yl)-9H-carbazol-9-yl)-N,N-diphenylaniline (PYR 1) exhibited high thermal stability, with decomposition temperatures of 425 °C and 400 °C, respectively. The triplet energy of PYR 1 (2.63 eV) was higher than that of TRZ 1 (2.44 eV), and facilitated suitable energy transfer to the green dopant. The PYR 1 based green device demonstrated an excellent maximum current efficiency of 48.7 cd/A and external quantum efficiency of 16.4%. Interestingly, the green device with PYR 1 showed an outstanding brightness of 95,870 cd/m2, which is three times greater than that of the reference CBP based device (31,370 cd/m2). The bipolar host PYR 1 is a promising material for high luminescent and low efficiency roll off applications, especially for green PhOLEDs.

Hole transporting material and Organic electroluminescent display device using the same

The hole transport material of claim 1, wherein the hole transport material is a hole transport material. Provided are an organic electroluminescent device and an electronic device including the same. Chemical Formula 1. Wherein R is as defined in the specification. The hole transport material has excellent external quantum efficiency, excellent luminous efficiency, brightness, thermal stability, and device lifetime, and can be easily used to produce OLED devices which are stable over a long term.

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

The present invention provides the compound represented by Formula 1, an organic electric element comprising a first electrode, a second electrode, and an organic material layer formed between the first electrode and the second electrode, and electronic d

Design and synthesis of quinoline-pyrimidine inspired hybrids as potential plasmodial inhibitors

Presently, artemisinin-based combination therapy (ACT) is the first-line therapy of Plasmodium falciparum malaria. With the emergence of malaria parasites that are resistant to ACT, alternative antimalarial therapies are urgently needed. In line with this

Discovery and mechanism of action studies of 4,6-diphenylpyrimidine-2-carbohydrazides as utrophin modulators for the treatment of Duchenne muscular dystrophy

Duchenne muscular dystrophy is a fatal disease with no cure, caused by lack of the cytoskeletal protein dystrophin. Upregulation of utrophin, a dystrophin paralogue, offers a potential therapy independent of mutation type. The failure of first-in-class utrophin modulator ezutromid/SMT C1100 in Phase II clinical trials necessitates development of compounds with better efficacy, physicochemical and ADME properties and/or complementary mechanisms. We have discovered and performed a preliminary optimisation of a novel class of utrophin modulators using an improved phenotypic screen, where reporter expression is derived from the full genomic context of the utrophin promoter. We further demonstrate through target deconvolution studies, including expression analysis and chemical proteomics, that this compound series operates via a novel mechanism of action, distinct from that of ezutromid.

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

The present invention relates to a novel heterocyclic compound and an organic light emitting element including the same as a light-emitting material and, more specifically, to a heterocyclic compound having excellent light emission properties, such as a driving voltage, light emission efficiency, and service life, and an organic light emitting element including the same. Since the heterocyclic compound according to the present invention is more stable compared to conventional materials and has the excellent light emission properties for the driving voltage or current efficiency, and service life, the organic light emitting element including the same can be more stably driven in a low-voltage and light emission efficiency can be improved.

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)

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.

Heterocyclic compounds and organic light-emitting diode including the same

The present invention relates to a new heterocyclic compound, and an organic electroluminescent device including the same as a light emitting material, specifically a heterocyclic compound denoted by chemical formula 1, and an organic electroluminescent device having excellent luminance properties including driving voltage and luminance efficiency.

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].