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Merck
CN

465089

Sigma-Aldrich

3,4-二氟苯硼酸

≥95%

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别名:
3,4-Difluorobenzeneboronic acid
线性分子式:
F2C6H3B(OH)2
分子量:
157.91
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

检测方案

≥95%

mp

305-310 °C (lit.)

SMILES字符串

OB(O)c1ccc(F)c(F)c1

InChI

1S/C6H5BF2O2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,10-11H

InChI key

RMGYQBHKEWWTOY-UHFFFAOYSA-N

应用

3,4-Difluorophenylboronic acid can be used as a reactant to prepare:
  • Fluorinated biaryl derivatives via Suzuki cross-coupling reaction with aryl and heteroaryl halides.
  • Flurodiarylmethanols by reacting with aryl aldehydes using Ni catalyst.
  • Conjugated fluorodiazaborinines by treating with diamines via intermolecular dehydration reaction for the detection of explosives.

Reactant involved in:
  • Suzuki cross-coupling reactions with aryl and heteroaryl halides
  • Oxo directing Liebeskind-Srogl cross-coupling reactions with gem-dihaloolefin-type α-oxo ketene dithioacetals
  • Substitution reactions with enyne acetates and carbonates

其他说明

含有不定量的酸酐

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Green synthesis of fluorinated biaryl derivatives via thermoregulated ligand/palladium-catalyzed Suzuki reaction
L Ning, et al.
Journal of Organometallic Chemistry, 696(13), 2641-2647 (2011)
Nickel salt-catalyzed addition reaction of arylboronic acids to aromatic aldehydes
Zhou L, et al.
Tetrahedron Letters, 50(4), 406-408 (2009)
NBN-Doped Conjugated Polycyclic Aromatic Hydrocarbons as an AIEgen Class for Extremely Sensitive Detection of Explosives
Wan W-M, et al.
Angewandte Chemie (International Edition in English), 57(47), 15510-15516 (2018)
Mingyan Jia et al.
Food chemistry, 335, 127566-127566 (2020-08-04)
In this work, we developed an optical colorimetric sensor array for the discrimination of Chinese teas. The sensor array was carefully designed based on tea polyphenol induced indicators displacement assay (IDA), using phenylboronic acids with different substituents as the receptors

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