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647292

Sigma-Aldrich

4-(Diphenylamino)phenylboronic acid

≥95%

Synonyme(s) :

4-(N,N-Diphenylamino)-1-phenylboronic acid, 4-(N,N-Diphenylamino)phenylboronic acid, 4-(N-Diphenylamino)phenylboronic acid, 4-(Diphenylamino)benzeneboronic acid, Triphenylamine-4-boronic acid

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About This Item

Formule empirique (notation de Hill):
C18H16BNO2
Numéro CAS:
201802-67-7
Poids moléculaire :
289.14
Numéro MDL:
MFCD06798117
Code UNSPSC :
12352103
ID de substance PubChem :
24883523
Nomenclature NACRES :
NA.22

Pureté

≥95%

Forme

powder

Pf

110-115 °C (lit.)

Chaîne SMILES 

OB(O)c1ccc(cc1)N(c2ccccc2)c3ccccc3

InChI

1S/C18H16BNO2/c21-19(22)15-11-13-18(14-12-15)20(16-7-3-1-4-8-16)17-9-5-2-6-10-17/h1-14,21-22H

Clé InChI

TWWQCBRELPOMER-UHFFFAOYSA-N

Catégories apparentées

Application

Reagent used for
  • Strong multiphoton-excited blue photoluminescence and lasing from ladder-type oligo(p-phenylene)s
  • Suzuki coupling reactions
  • Ligand-free Suzuki reaction

Reagent used in Preparation of
  • Push-pull arylvinyldiazine chromophores
  • Benzothiadiazole-based fluorophores contg. triphenylamine functionality
  • Blue light-emitting and hole-transporting materials for electroluminescent devices
  • p-quaterphenyls laterally substituted with dimesitylboryl group for use as solid-state blue emitters
  • Efficient sensitizers for dye-sensitized solar cells
  • Prange electroluminescent materials for single-layer white polymer OLEDs
  • Eeep-blue organic light emitting devices (OLEDs)
  • Ligands for Organic Photovoltaic cells

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Consulter la Bibliothèque de documents

High Efficiency Nondoped Deep-Blue Organic Light Emitting Devices Based on Imidazole-p-triphenylamine Derivatives
Zhang, Y.; et al.
Chemistry of Materials, 24, 61-70 (2012)
Synthesis and characterizations of benzothiadiazole-based fluorophores as potential wavelength-shifting materials
Li, Y.; et al.
J. Photochem. Photobiol., A, 231, 51-59 (2012)
Effect of main ligands on organic photovoltaic performance of Ir(III) complexes
Lee, W.; et al.
New. J. Chem., 35, 2557-2563 (2011)
Blue light-emitting and hole-transporting materials based on 9,9-bis(4-diphenylaminophenyl)fluorenes for efficient electroluminescent devices
Thangthong, A.-M.; et al.
Journal of Materials Chemistry, 22, 6869-6877 (2012)
Ziyang He et al.
Journal of colloid and interface science, 567, 136-144 (2020-02-12)
Fluorescence imaging and magnetic resonance imaging have been research hotspots for adjuvant therapy and diagnosis. However, traditional fluorescent probes or contrast agents possess insurmountable weaknesses. In this work, we reported the preparation of dual-mode probes based on mesoporous silica nanomaterials
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