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900517

Sigma-Aldrich

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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About This Item

经验公式（希尔记法）:
C26H21BO2
CAS号:
1227040-87-0
分子量:
376.25
MDL號碼:
MFCD30537204
分類程式碼代碼:
12352106
PubChem物質ID:
329769835
NACRES:
NA.23

化驗

97%

品質等級

100

形狀

powder

mp

126-131 °C

SMILES 字串

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 密鑰

XSIVQWOJIOHPIZ-UHFFFAOYSA-N

相关类别

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCB8335

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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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