900517
B-[4-(1,2,2-Triphenylethenyl)phenyl]boronic acid
别名:
1,2,2-Triphenylethenyl-(4′-phenylene) boronic acid, [4-(1,2,2-Triphenylvinyl)phenyl]boronic acid
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关于此项目
经验公式（希尔记法）:
C26H21BO2
化学文摘社编号:
分子量:
376.25
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.23
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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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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