1169709-19-6

Basic information

• Product Name: 2-Phenyl-1-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-benzoiMidazole
• Synonyms: 2-Phenyl-1-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-benzoiMidazole;2-phenyl-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1Hbenzo[d]imidazole
• CAS NO: 1169709-19-6
• Molecular Formula: C₂₅H₂₅BN₂O₂
• Molecular Weight: 396.2892
• EINECS: 200-258-5
• Mol File: 1169709-19-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 564.0±52.0 °C(Predicted)
• Appearance: /
• Density: 1.12±0.1 g/cm3(Predicted)
• PKA: 4.03±0.10(Predicted)
• CAS DataBase Reference: 2-Phenyl-1-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-benzoiMidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenyl-1-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-benzoiMidazole(1169709-19-6)
• EPA Substance Registry System: 2-Phenyl-1-[4-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-benzoiMidazole(1169709-19-6)

Safety Data

• Hazardous Substances Data: 1169709-19-6(Hazardous Substances Data)

Usage

General Description

2-Phenyl-1-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-benzimidazole is a complex organic compound with a molecular structure containing a benzimidazole ring, a phenyl group, and a boron-containing moiety. The compound has potential applications in medicinal chemistry and material science due to its unique structural features and potential pharmacological properties. Specifically, the boron-containing group in the molecule may contribute to its reactivity and ability to interact with biological targets. Further research is needed to fully understand the potential uses and properties of this chemical.

Upstream product

• 760212-58-6 4-(2-phenyl-1H-benzo[d]imidazol-1-yl)1-bromobenzene 
• 73183-34-3 bis(pinacol)diborane 
• 760212-57-5 N-[2-(4-bromophenyl amino) phenyl] benzamide 
• 100-52-7 benzaldehyde 
• 100953-52-4 N¹-(4-bromophenyl)benzene -1,2 -diamine 
• 58476-59-8 4-bromo-N-(2-nitrophenyl)benzenamine 
• 106-40-1 4-bromo-aniline 
• 1493-27-2 ortho-nitrofluorobenzene 

Downstream Products

• 1169709-20-9 C₃₃H₂₂N₂ 
• 1599466-11-1 N,N-diphenyl-4'-(4-(2-phenyl-1H-benzo[d]imidazol-1-yl)phenyl)-[1,1'-binaphthalen]-4-amine 
• 1449412-25-2 9-phenyl-3-{3-[4-(2-phenyl-1H-benzo[d]imidazol-1-yl)phenyl]-9-para-tolyl-9H-fluoren-9-yl}-9H-carbazole 
• 1407503-35-8 C₅₆H₃₅N₃ 
• 1407502-90-2 C₄₄H₂₉N₃ 
• 1383795-79-6 C₅₂H₃₃N₃ 

Relevant articles and documents

Compounds comprising benzophenone group, Organic electronic device comprising organic layers comprising the photo-cured of the monomer compounds

The compound represented by Formula I or II is provided as an organic material layer material of an organic electronic device. The benzophenone functional group-containing compound represented by the following Chemical I or Chemical Formula II: I (Chemical Formula Ar -) (R). 1 -R2 -Bpm In the formula, m is 1 and 10, and Ar is a substituted or unsubstituted m having a C-order linking group. 6 -C60 Substituted or unsubstituted m having aryl group, C nd-linking group3 -C60 Substituted or unsubstituted fused m with heteroaryl groups or C primary linking groups6 -C60 Aryl group, R1 And R2 Each independently represents a simple bond, O - a substituted or unsubstituted C. 6 -C30 Arylene group, substituted or unsubstituted C3 -C30 Heteroarylene group, substituted or unsubstituted C1 -C10 The alkylene group and Bp are 1 divalent linking groups derived from benzophenone functional groups. Chemical Formula II. In the formula, n is at least 1 and Ar ' is a substituted or unsubstituted m having a C-order linking group. 6 -C60 Aryl group Substituted or unsubstituted m having a C nd order linker3 -C60 Substituted or unsubstituted fused m with heteroaryl groups or C primary linking groups6 -C60 Aryl group, R3 And R4 Each independently represents a simple bond, O - a substituted or unsubstituted C. 6 -C30 Arylene group, substituted or unsubstituted C3 -C30 Heteroarylene group, substituted or unsubstituted C6 -C30 Fused arylene groups, substituted or unsubstituted C1 -C10 The alkylene group and Bp ' are 1 divalent linking groups derived from benzophenone functional groups.

Monomer compounds comprising uracil group, Organic layers comprising the cross-linked of the monomer compounds, and Organic electronic device comprising the organic layers

The present invention provides a pyrimidine-based functional group-containing monomolecular compound represented by chemical formula 1 of Ar-(R_1-R_2-Py)_n as a material for an organic layer of an organic electronic device. The compound can form an organic layer within a short time through photo-curing at room temperature. In chemical formula 1, n is 2-10; Ar is a substituted or non-substituted C_6-C_60 aryl group, or a substituted or non-substituted C_3-C_60 heteroaryl group having an n-valent linking group; each of R_1 and R_2 independently represents a single bond, -O-, a substituted or non-substituted C_6-C_30 arylene group, a substituted or non-substituted C_3-C_30 heteroarylene group, a substituted or non-substituted C_1-C_10 alkylene group, a substituted or non-substituted C_1-C10 alkoxylene group, a substituted or non-substituted amide group, or a substituted or non-substituted amine group; and Py is a monovalent linking group derived from a pyrimidine-based functional group.COPYRIGHT KIPO 2020

Substituted 1,3,5-triazine compound, composition and application thereof

The invention discloses a substituted 1,3,5-triazine compound, a composition and application thereof. The 1,3,5-triazine compound shown as a formula I is provided by the invention, can be used as an electron transport material and, can be used as an electron acceptor material. The composition that can be used for preparing an electron transport layer or an electron donor material is used as a mainbody material of an electroluminescent device, so that the prepared electroluminescent device has the advantages of relatively high efficiency, relatively long service lifetime and the like. As the 1,3,5-triazine compound is used as an electron transport layer, the composition used as an electron acceptor material and an electron donor material is adopted to construct a light-emitting layer, andthe prepared electroluminescent device has the advantages of higher efficiency, longer service lifetime and the like.