74065-48-8

Basic information

• Product Name: 4-methyl-N-p-tolyl-N-(4-vinylphenyl)benzenamine
• Synonyms: 4-methyl-N-p-tolyl-N-(4-vinylphenyl)benzenamine
• CAS NO: 74065-48-8
• Molecular Weight: 299.415
• Mol File: 74065-48-8.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 4-methyl-N-p-tolyl-N-(4-vinylphenyl)benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-p-tolyl-N-(4-vinylphenyl)benzenamine(74065-48-8)
• EPA Substance Registry System: 4-methyl-N-p-tolyl-N-(4-vinylphenyl)benzenamine(74065-48-8)

Safety Data

• Hazardous Substances Data: 74065-48-8(Hazardous Substances Data)

Upstream product

• 106-43-4 para-chlorotoluene 
• 1520-21-4 4-vinyl benzylamine 
• 106-38-7 para-bromotoluene 
• 624-31-7 4-tolyl iodide 
• 42906-19-4 4-[N,N-di(p-tolyl)amino]benzaldehyde 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 20440-95-3 N-phenyl-di-p-tolylamine 
• 101089-53-6 4-[N,N-di(p-tolyl)amino]benzaldehyde 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Downstream Products

• 1169701-28-3 2-cyano-3-(4-{2-[4-(di-p-tolylamino)phenyl]vinyl}phenyl)acrylic acid 
• 1118129-08-0 trans-4-formyl-4'-(N,N-bis(4-methylphenyl)amino)-stilbene 
• 1355320-79-4 1-[4-(di-(p-tolyl)amino)phenyl]-3-(triphenyl)phosphoniumpropyl-1-ene bromide 
• 1610043-93-0 C₂₇H₂₅NO 
• 1610043-98-5 C₂₆H₂₅N 
• 1610043-92-9 C₂₅H₂₃NO 
• 1610043-97-4 C₂₄H₂₃N 
• 1610043-96-3 C₆₈H₆₀N₂ 
• 1610043-95-2 C₆₄H₅₆N₂ 
• 1610043-94-1 C₆₀H₅₂N₂ 
• 925452-57-9 (E)-3-(4-(di-p-tolylamino)phenyl)acrylaldehyde 
• 1428113-81-8 (E)-3-(5-(3,5-bis((1E,3E)-4-(4-(di-p-tolylamino)phenyl)buta-1,3-dienyl)-4-(octyloxy)phenyl)-3-hexylthiophen-2-yl)-2-cyanoacrylic acid 
• 1428113-78-3 5-(3,5-bis((1E,3E)-4-(4-(di-p-tolylamino)phenyl)buta-1,3-dienyl)-4-(octyloxy)phenyl)-3-hexylthiophene-2-carbaldehyde 
• 1428113-76-1 N-(4-((1E,3E)-4-(5-bromo-3-((1E,3E)-4-(4-(di-p-tolylamino)phenyl)buta-1,3-dienyl)-2-(octyloxy)phenyl)buta-1,3-dienyl)phenyl)-4-methyl-N-p-tolylbenzenamine 

Relevant articles and documents

Aromatic pyridazine compound as well as preparation method and application thereof (by machine translation)

The invention discloses an aromatic pyridazine compound and a use thereof. 1 H-NMR and the like are characterized in that the compound has a longer charge-off-state life and can be used as a better photoelectric material. In addition, the invention further provides a preparation method of the aromatic pyridazine compound, and the preparation method is environment-friendly and convenient to operate. The method comprises the following steps: Step 1, reacting 2 and 4 - dibromonitrobenzene as raw materials through coupling reaction, 5, 5 - dibromo -2, 2 ’ -dinitrobiphenyl, step 2 and taking R1 The substituted ethylene derivatives and 5, 5 - dibromo -2 and 2 ’ -dinitrobiphenyl serve as raw materials to synthesize nitro-substituted compounds through coupling reaction; step 3: synthesizing an aromatic pyridazine compound by a reduction reaction with the nitro-substituted compound as a raw material. The invention further discloses application of the aromatic pyridazine compound in a solar cell and application of the aromatic pyridazine compound in pH detection. (by machine translation)

Block copolymers for directional charge transfer: Synthesis, characterization, and electrochemical properties of redox-active triarylamines

A series of styrenic triarylamines bearing electron-withdrawing or electron-donating substituents were synthesized and readily polymerized by nitroxide-mediated polymerization (NMP). The utility of the homopolymers as macroinitiators for the preparation o

Novel hole transporting materials with a linear π-conjugated structure for highly efficient perovskite solar cells

Novel small-molecule hole transporting materials (HTMs) with a linear π-conjugated structure have been synthesized. The perovskite solar cell based on 2TPA-2-DP as the HTM exhibits an encouraging power conversion efficiency of 9.1% under AM 1.5 G (100 mW cm-2) illumination, which is the first demonstration of an effective perovskite solar cell using a linear structured HTM. This journal is the Partner Organisations 2014.