343239-58-7

Basic information

• Product Name: 3',5'-diphenylbiphenyl-4-aMine
• Synonyms: 3',5'-diphenylbiphenyl-4-aMine;4-AMino-3',5'-diphenylbiphenyl, 98%;5'-Phenyl-[1,1':3',1''-terphenyl]-4-aMine
• CAS NO: 343239-58-7
• Molecular Formula: C₂₄H₁₉N
• Molecular Weight: 321.41436
• Mol File: 343239-58-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 138-139℃
• Boiling Point: 505℃
• Flash Point: 275℃
• Appearance: /
• Density: 1.117
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.24±0.10(Predicted)
• CAS DataBase Reference: 3',5'-diphenylbiphenyl-4-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 3',5'-diphenylbiphenyl-4-aMine(343239-58-7)
• EPA Substance Registry System: 3',5'-diphenylbiphenyl-4-aMine(343239-58-7)

Safety Data

• Hazardous Substances Data: 343239-58-7(Hazardous Substances Data)

Usage

General Description

3',5'-diphenylbiphenyl-4-aMine is a chemical compound, although there is limited information and metadata about it. It may fall into the biphenyl category, which consists of molecules with two phenyl rings connected by a single standard bond. Generally, biphenyls are used for a variety of applications, including heat transfer fluids, plant growth regulators, and synthesis of pharmaceuticals. It's crucial to note that the properties, uses, or potential health effects of 3',5'-diphenylbiphenyl-4-aMine specifically are not well documented, possibly due to it being an unfamiliar or rare compound. For further information about this chemical, it would be advisable to have a complete and accurate IUPAC name or a CAS registry number.

Upstream product

• 118727-34-7 1,3,5-tris(4-aminophenyl)benzene 
• 3816-12-4 4'-nitro-5'-phenyl-1,1':3',1''-terphenyl 
• 1222-98-6 4-nitrochalcone 
• 98124-35-7 4-nitro-[1,1':3',1-terphenyl]-5'-phenol 
• 555-16-8 4-nitrobenzaldehdye 
• 1384480-20-9 3,5-diphenylphenyl trifluoromethanesulfonate 
• 98-86-2 acetophenone 
• 94-41-7 benzalacetophenone 
• 28023-86-1 3,5-diphenylphenol 
• 626-39-1 1,3,5-trisbromobenzene 
• 98-80-6 phenylboronic acid 
• 5419-55-6 Triisopropyl borate 
• 103068-20-8 1-bromo-3,5-diphenylbenzene 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 116941-51-6 4-chloro-5′-phenyl-1,1′:3′,1″-terphenyl 

Relevant articles and documents

Quantitative treatment of surface potentials in Langmuir films from aromatic amphiphiles

It is shown that the surface potentials of Langmuir monolayers from aromatic compounds can be interpreted using the three-layer capacitor model of Demchak and Fort, with the same local dielectric constants employed for aliphatic compounds. Based on new da

Azo bond formation on metal surfaces

The formation of azo compounds via redox cross-coupling of nitroarenes and arylamines, challenging in solution phase chemistry, is achieved by on-surface chemistry. Reaction products are analyzed with a cryogenic scanning tunneling microscope (STM) and X-ray photoelectron spectroscopy (XPS). By using well-designed precursors containing both an amino and a nitro functionality, azo polymers are prepared on surface via highly efficient nitro-amino cross-coupling. Experiments conducted on other substrates and surface orientations reveal that the metal surface has a significant effect on the reaction efficiency. The reaction was further found to proceed from partially oxidized/reduced precursors in dimerization reactions, shedding light on the mechanism that was studied by DFT calculations.

A halogen substituted of compounds of preparation method

The invention discloses a type 1 shown of compounds of halogen substituted preparation method, comprises the following steps: (1) condensation reaction: (2) Cyclization reaction: (3) The substitution reaction: (4) Coupling reaction: (5) Reduction reaction: (6) The diazotization reaction: Wherein X is selected from F, Cl, Br, I.