Accéder au contenu
Merck
Toutes les photos(1)

Documents

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

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
Toutes les photos(1)

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)

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Hai Hua Fan et al.
Journal of the American Chemical Society, 134(17), 7297-7300 (2012-04-24)
We report the synthesis and investigation of multiphoton absorption properties of a novel series of diphenylamino-end-capped ladder-type oligo(p-phenylene)s which exhibit greatly enhanced and efficient multiphoton (from two- to five-photon) upconverted blue photoluminescence with which the record-high intrinsic three-photon absorption cross-section
Synthesis and characterization of 9,10-substituted anthracene derivatives as blue light-emitting and hole-transporting materials for electroluminescent devices
Thangthong, A-M.; et al.
Tetrahedron, 68, 1853-1861 (2012)
Highly efficient single-layer white polymer light-emitting devices employing triphenylamine-based iridium dendritic complexes as orange emissive component
Zhu, M.; et al.
Journal of Materials Chemistry, 22, 361-366 (2012)
Woochul Lee et al.
Chemistry, an Asian journal, 7(2), 343-350 (2011-12-14)
We have synthesized and characterized four organic dyes (H1-H4) based on a 3,6-disubstituted carbazole donor as sensitizers in dye-sensitized solar cells. These dyes have high molar extinction coefficients and energy levels suitable for electron transfer from an electrolyte to nanocrystalline
Sompit Wanwong et al.
Materials (Basel, Switzerland), 13(12) (2020-06-19)
Two boron dipyrromethene (BODIPY) triads, namely BODIPY-1 and BODIPY-2, were synthesized and incorporated with poly-3-hexyl thiophene: (6,6)-phenyl-C61-butyric acid methyl ester (PCBM) P3HT:PCBM. The photovoltaic performance of BODIPY:P3HT:PCBM ternary solar cells was increased, as compared to the control binary solar cells
Afficher tous les articles scientifiques apparentés

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique