41604-22-2

Basic information

• Product Name: 4-Bromobiphenyl-2-amine
• Synonyms: 4-Bromobiphenyl-2-amine
• CAS NO: 41604-22-2
• Molecular Formula: C₁₂H₁₀BrN
• Molecular Weight: 248.12
• Mol File: 41604-22-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 203-205 °C(Press: 10.5 Torr)
• Appearance: /
• Density: 1.432±0.06 g/cm3(Predicted)
• PKA: 2.74±0.10(Predicted)
• CAS DataBase Reference: 4-Bromobiphenyl-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromobiphenyl-2-amine(41604-22-2)
• EPA Substance Registry System: 4-Bromobiphenyl-2-amine(41604-22-2)

Safety Data

• Hazardous Substances Data: 41604-22-2(Hazardous Substances Data)

Upstream product

• 3460-18-2 1,4-dibromo-2-nitrobenzene 
• 98-80-6 phenylboronic acid 
• 112671-42-8 4-bromo-1-iodo-2-nitrobenzene 
• 64085-52-5 5-bromo-2-iodo-aniline 
• 71-43-2 benzene 
• 70873-41-5 4-bromo-2-nitro-1-phenylbenzene 
• 3638-73-1 2,5-dibromoaniline 

Downstream Products

• 1616458-78-6 1-azabicyclo[2.2.2]oct-4-yl (4-bromobiphenyl-2-yl)carbamate 
• 1616458-57-1 1-azabicyclo[2.2.2]oct-4-yl [4-(4-{[2-chloro-4-(hydroxymethyl)-5-methoxyphenyl]-amino}-4-oxobutyl)biphenyl-2-yl]carbamate 
• 1616458-56-0 ethyl 4-{[4-(2-{[(1-azabicyclo[2.2.2]oct-4-yloxy)carbonyl]amino}biphenyl-4-yl)butanoyl]amino}-5-chloro-2-methoxybenzoate 
• 41604-19-7 1-bromo-3-fluoro-4-phenylbenzene 

Relevant articles and documents

LIPOXYGENASE INHIBITORS

Various embodiments of the present disclosure are directed to compounds having Formula (I), Formula (IA), Formula (IB), Formula (IC), Formula (ID), Formula (IE), and/or pharmaceutically acceptable salts thereof. The compounds can be suitable for inhibiting lipoxygenases, and/or treating associated diseases, such as Alzheimer's disease. In some embodiments, the compounds may be administered to a patient as part of a pharmaceutical formulation.

Electrochemical Palladium-Catalyzed Intramolecular C—H Amination of 2-Amidobiaryls for Synthesis of Carbazoles

The synthesis of carbazoles based on the electrochemical Pd-catalyzed intramolecular C—H amination of 2-amidobiaryls through oxidative cross coupling has been achieved under mild reaction conditions. The reaction can be carried out in undivided cell without the addition of external chemical oxidant. Besides good functional group compatibility, the desired carbazoles can be scaled up and modified easily. Compared with previous methods, this protocol affords a simple and sustainable avenue for the construction of carbazoles.

A compound. Hole transporting material, organic electroluminescent device and display device (by machine translation)

The invention provides a compound of general formula (I). It can be used for hole transport materials. The compound has the fluorene fused ring-linked ortho-substituted phenyl triarylamine parent structure, the bond between atoms can be high, good thermal stability is achieved, solid deposition between molecules is facilitated, and the transition capability of holes is high. Be applied to hole transport layer, have suitable energy level level between adjacent level, be favorable to the injection and the migration of hole, can effectively reduce drive voltage, higher hole mobility simultaneously, can effectively promote organic electroluminescence device's luminous efficiency. The invention also provides a hole transport material comprising the compound of the general formula (I). Organic electroluminescent device and display device. (by machine translation)