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
CAS Number:
分子量:
376.25
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.23
方案
97%
质量水平
表单
powder
mp
126-131 °C
SMILES字符串
B(O)(O)c1ccc(cc1)C(=C(c4ccccc4)c3ccccc3)c2ccccc2
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
InChI key
XSIVQWOJIOHPIZ-UHFFFAOYSA-N
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
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)
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
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
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