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Merck
CN

721433

Sigma-Aldrich

4-Ethynylphenylboronic acid pinacol ester

95%

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别名:
2-(4-Ethynylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
经验公式(希尔记法):
C14H17BO2
分子量:
228.09
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

95%

形式

solid

mp

66-70 °C

SMILES字符串

CC1(C)OB(OC1(C)C)c2ccc(cc2)C#C

InChI

1S/C14H17BO2/c1-6-11-7-9-12(10-8-11)15-16-13(2,3)14(4,5)17-15/h1,7-10H,2-5H3

InChI key

LOVNTFMVZVIASV-UHFFFAOYSA-N

应用

4-Ethynylphenylboronic acid pinacol ester can be used:
  • For the functionalization of platinum nanoparticles to leverage their photoluminescence properties.
  • As an intermediate in the synthesis of covalent heterodyads of chlorophyll derivatives applicable as supramolecular light-harvesting systems.
  • As an intermediate in the preparation of F-18 radiolabeled galectin-3 inhibitors, which are used as surrogate positron emission tomography (PET) tracers of TD139 and GB1107.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Covalent heterodyads of synthetic chlorophyll derivatives linked with linear rigid substituents at the 20-positions constructing photoexcited energy transfer systems
Shoji S, et al.
Tetrahedron, 76(17), 131130-131130 (2020)
Platinum nanoparticles functionalized with ethynylphenylboronic acid derivatives: selective manipulation of nanoparticle photoluminescence by fluoride ions
Hu P, et al.
Langmuir, 30(18), 5224-5229 (2014)
In Vivo Veritas: 18F-Radiolabeled Glycomimetics Allow Insights into the Pharmacological Fate of Galectin-3 Inhibitors
Bratteby K, et al.
Journal of Medicinal Chemistry, 63(2), 747-755 (2019)

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