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900517

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

Name: B-[4-(1,2,2-Triphenylethenyl)phenyl]boronic acid
Brand: ALDRICH

同義詞:

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

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About This Item

經驗公式（希爾表示法）:

C₂₆H₂₁BO₂

CAS號碼:

1227040-87-0

分子量：:

376.25

分類程式碼代碼:

12352106

PubChem物質ID:

329769835

NACRES:

NA.23

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Sigma-Aldrich

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4-氨基苯硼酸盐酸盐

化驗

97%

品質等級

100

形狀

powder

mp

126-131 °C

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

分析證明 (COA)

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Effect of AIE substituents on the fluorescence of tetraphenylethene-containing BODIPY derivatives.

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

Biocompatible Green and Red Fluorescent Organic Dots with Remarkably Large Two-Photon Action Cross Sections for Targeted Cellular Imaging and Real-Time Intravital Blood Vascular Visualization.

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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Key Documents

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

About This Item

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屬性

化驗

品質等級

形狀

mp

相關類別

安全資訊

儲存類別代碼

水污染物質分類（WGK）

閃點（°F）

閃點（°C）

文件

分析證明 (COA)

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