2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole

What We Offer

2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole

2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole | 852-38-0

Catalog Number A17-0112
Category Laser Dyes
Molecular Formula C20H14N2O
Molecular Weight 298.345
Catalog Number Size Price Quantity
A17-0112 -- $--

Product Introduction

2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole is a small-molecule laser dye.

Chemical Information

Synonyms 2-[1,1'-biphenyl]-4-yl-5-phenyl-1,3,4-oxadiazole; 2-Phenyl-5-(4-biphenylyl)-1,3,4-oxadiazole; PBD
IUPAC Name 2-phenyl-5-(4-phenylphenyl)-1,3,4-oxadiazole
Canonical SMILES C1=CC=C(C=C1)C2=CC=C(C=C2)C3=NN=C(O3)C4=CC=CC=C4
InChI InChI=1S/C20H14N2O/c1-3-7-15(8-4-1)16-11-13-18(14-12-16)20-22-21-19(23-20)17-9-5-2-6-10-17/h1-14H
InChI Key WMAXWOOEPJQXEB-UHFFFAOYSA-N
  • Application

2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole, a versatile heterocyclic organic compound, finds extensive applications in diverse scientific and industrial settings. Explore the manifold uses of this compound, presented with heightened perplexity and burstiness.

Organic Light-Emitting Diodes (OLEDs): Serving as a cornerstone in OLED technology, this compound stands out as an electroluminescent material renowned for its exceptional thermal and chemical stability. Its deployment in display screens and lighting applications showcases its prowess, with OLEDs incorporating this material, boasting remarkable luminance, expansive color gamut, and heightened energy efficiency.

Fluorescent Probes: Witness the transformative impact of 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole in the realm of fluorescent probes designed for cutting-edge biological imaging and diagnostic ventures. Relying on its robust fluorescence attributes, these probes enable real-time visualization of intricate cellular processes, playing an instrumental role in unraveling molecular interactions, pinpointing cellular markers, and dissecting dynamic biological systems with precision.

Organic Photovoltaics: Embrace the frontier of solar energy with the utilization of this compound in crafting organic photovoltaic solar cells, where it serves as an electron-transporting linchpin. Boasting an elevated electron affinity and robust charge mobility, this compound fuels the seamless conversion of solar energy into usable power. Organic photovoltaics incorporating this compound present a flexible, lightweight, and cost-effective alternative to conventional silicon-based solar panels.

Chemical Sensors: Delve into the realm of sensor technology with the incorporation of 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole in the development of advanced chemosensors and biosensors tailored for detecting an array of substances, from noxious metals to intricate biological compounds. Its unparalleled sensitivity and selectivity position it as a vital tool in environmental monitoring and medical diagnostics, offering a precise and swift detection mechanism that enables timely interventions and fosters a proactive approach to safeguarding health and the environment.

Computed Properties

XLogP3 4.7
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 3
Exact Mass 298.110613074 g/mol
Monoisotopic Mass 298.110613074 g/mol
Topological Polar Surface Area 38.9Ų
Heavy Atom Count 23
Formal Charge 0
Complexity 355
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

Patents

Publication NumberTitlePriority Date
RU-2767518-C1 Method of producing para-terphenyl of scintillation quality 2021-08-20
JP-2022163324-A Plastic scintillator and manufacturing method thereof 2021-04-14
WO-2022160875-A1 Functional material, light emitting substrate and preparation method therefor, and light emitting apparatus 2021-01-27
WO-2022161959-A1 Devices and methods for detecting gamma radiation 2021-01-26
NL-2026928-B1 NPE-free LSC cocktail compositions suitable for Low Level applications. 2020-11-19
cartIcon
Inquiry Basket