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Merck
모든 사진(1)

주요 문서

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647292

Sigma-Aldrich

4-(Diphenylamino)phenylboronic acid

≥95%

동의어(들):

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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모든 사진(1)

About This Item

실험식(Hill 표기법):
C18H16BNO2
CAS Number:
201802-67-7
Molecular Weight:
289.14
MDL number:
MFCD06798117
UNSPSC 코드:
12352103
PubChem Substance ID:
24883523
NACRES:
NA.22

Quality Level

100

분석

≥95%

형태

powder

mp

110-115 °C (lit.)

SMILES string

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

InChI key

TWWQCBRELPOMER-UHFFFAOYSA-N

관련 카테고리

애플리케이션

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number
SHBN1284
SHBH1277V
16796BMV
SHBB6347V
16796BM

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COA 검색

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문서 라이브러리 방문

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
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
Guang-Liang Fu et al.
The Journal of organic chemistry, 77(4), 1983-1990 (2012-01-21)
A new family of p-quaterphenyls 1-6 laterally substituted with a bulky electron-accepting dimesitylboryl group has been designed and synthesized. These compounds were characterized by X-ray crystallography, UV-vis and fluorescence spectroscopy, and DFT calculations as well as thermogravimetric analysis (TGA), differential
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)
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