22082-94-6

Basic information

• Product Name: 2-broMo-6-phenylnaphthalene
• Synonyms: 2-broMo-6-phenylnaphthalene;6-phenyl-2-bromonaphthalene
• CAS NO: 22082-94-6
• Molecular Formula: C₁₆H₁₁Br
• Molecular Weight: 283.16254
• Mol File: 22082-94-6.mol

Chemical Properties

• Melting Point: 132 °C
• Boiling Point: 398.5±11.0 °C(Predicted)
• Appearance: /
• Density: 1.381±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-broMo-6-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-broMo-6-phenylnaphthalene(22082-94-6)
• EPA Substance Registry System: 2-broMo-6-phenylnaphthalene(22082-94-6)

Safety Data

• Hazardous Substances Data: 22082-94-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-Bromo-6-phenylnaphthalene is utilized as a building block in organic synthesis for the preparation of a wide range of pharmaceuticals, agrochemicals, and other functional materials. Its unique structure makes it a valuable component in creating new and effective compounds.
Used in Synthesis of Biologically Active Compounds:
2-broMo-6-phenylnaphthalene also serves as a reagent in the synthesis of biologically active compounds, contributing to the development of new drugs and therapies.
Used in Medicinal Chemistry:
2-Bromo-6-phenylnaphthalene has potential applications in medicinal chemistry, where it can be used to design and develop novel pharmaceuticals with improved properties and therapeutic effects.
Used in Material Science:
In the field of material science, 2-broMo-6-phenylnaphthalene may be employed to create new materials with specific characteristics, such as improved stability or reactivity.
Safety Precautions:
It is crucial to handle 2-bromo-6-phenylnaphthalene with care, as it is a potential irritant to the skin, eyes, and respiratory system. Proper safety measures should be taken when working with 2-broMo-6-phenylnaphthalene to minimize any adverse effects.

Upstream product

• 71590-32-4 N-(6-bromo-[2]naphthyl)-acetamide 
• 389806-32-0 2-bromo-6-iodo-naphthalene 
• 98-80-6 phenylboronic acid 
• 15231-91-1 6-bromo-naphthalen-2-ol 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 151600-02-1 6-bromo-2-naphthalenyl trifluoromethanesulfonate 
• 591-50-4 iodobenzene 
• 1337916-18-3 (6-bromonaphthalene-2-yl)boronic acid 
• 13720-06-4 2,6-dibromonaphthalene 
• 100-58-3 phenylmagnesium bromide 
• 71-43-2 benzene 

Downstream Products

• 1337916-19-4 3,5-dimethyl-2-(6-phenylnaphthalen-2-yl)pyrazine 
• 1300028-96-9 N-6-diphenylnaphthalen-2-amine 
• 876442-90-9 (6-phenylnaphthalen-2-yl)boronic acid 

Relevant articles and documents

Amine compound and organic electroluminescent device including the same

An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and a plurality of organic layers disposed between the first electrode and the second electrode, wherein at least one among the plurality of organic layers includes an amine compound represented by Formula 1a, thereby showing excellent emission efficiency and/or improved life characteristics:

ORGANIC ELECTROLUMINESCENT COMPOUND, A PLURALITY OF HOST MATERIALS, AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

An organic electroluminescent compound. 1 Is a cross-1 sectional view of 1 an organic electroluminescent 2 device according to an embodiment of the present invention to provide an organic electroluminescent device having improved driving voltage, light emitting efficiency, power efficiency, and/or lifespan properties by including the organic electroluminescent compound according to the present invention as a single host material or a specific combination of compounds according to the present invention.

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Preparation of novel fused ring spiro[benzotetraphene-fluorene] derivatives and application for deep-blue host materials

A series of novel fused-ring spiro compounds, spiro[benzo[ij]tetraphene-7, 9′-fluorene] (SBTF) derivatives containing an end-capping aryl substituent at both the C3 and C10-positions hasbeen designed and synthesized via multi-step Suzuki coupling reactions. 3-(1-Naphthyl)-10-phenylSBTF (1N-PSBTF), 3-(2-naphthyl)-10-phenylSBTF (2N-PSBTF) and 3-[4-(1-naphthyl)phenyl]-10- phenylSBTF (NP-PSBTF) showed improved glass transition temperatures (T g) with good thermal stability. Their photophysical, electrochemical, and electroluminescent properties were investigated and were used to construct blue organic light emission diodes (OLEDs). The typical OLED devices showed excellent performance; the NP-PSBTF-based device exhibited highly efficient deep blue-light emission with a maximum efficiency of 5.27 cd/A (EQE, 4.63%) with CIE (x = 0.133, y = 0.144). According to these characteristics, these deep-blue light emitting materials have sufficient potential for fluorescent OLED applications.

Organometallic Complex, Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device

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ANTHRACENE DERIVATIVES, ORGANIC ELECTRONIC DEVICES USING ANTHRACENE DERIVATIVES, AND ELECTRONIC APPARATUSES COMPRISING ORGANIC ELECTRONIC DEVICE

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NEW ANTHRACENE DERIVATIVES, PREPARATION METHOD THEREOF AND ORGANIC LIGHT EMITTING DIODE USING THE SAME

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ANTHRYLARYLENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

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