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Merck
CN

900517

B-[4-(1,2,2-Triphenylethenyl)phenyl]boronic acid

Synonym(s):

1,2,2-Triphenylethenyl-(4′-phenylene) boronic acid, [4-(1,2,2-Triphenylvinyl)phenyl]boronic acid

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About This Item

Empirical Formula (Hill Notation):
C26H21BO2
CAS Number:
Molecular Weight:
376.25
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.23
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InChI key

XSIVQWOJIOHPIZ-UHFFFAOYSA-N

InChI

1S/C26H21BO2/c28-27(29)24-18-16-23(17-19-24)26(22-14-8-3-9-15-22)25(20-10-4-1-5-11-20)21-12-6-2-7-13-21/h1-19,28-29H

SMILES string

B(O)(O)c1ccc(cc1)C(=C(c4ccccc4)c3ccccc3)c2ccccc2

assay

97%

form

powder

mp

126-131 °C

Quality Level

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Cesar F Azael Gomez-Duran et al.
ACS applied materials & interfaces, 7(28), 15168-15176 (2015-06-26)
A series of BODIPY derivatives with tetraphenylethene (TPE) moieties were designed and synthesized. The effect of positions and numbers of substitution groups on the fluorescence of the BODIPYs was investigated. Theoretical calculation and single crystal structures proved that the TPE
Jiayun Xiang et al.
ACS applied materials & interfaces, 7(27), 14965-14974 (2015-06-23)
Fluorescent organic dots are emerging as promising bioimaging reagents because of their high brightness, good photostability, excellent biocompatibility, and facile surface functionalization. Organic dots with large two-photon absorption (TPA) cross sections are highly desired for two-photon fluorescence microscopy. In this
Effect of the cyano group on solid state photophysical behavior of tetraphenylethene substituted benzothiadiazoles.
Jadhav T, et al.
Journal of Material Chemistry C, 3(35), 9063-9068 (2015)

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