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Merck
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文件

445223

Sigma-Aldrich

2-氟苯硼酸

≥95%

同義詞:

2-Fluorobenzeneboronic acid, o-fluoro-benzeneboronic acid

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About This Item

線性公式:
FC6H4B(OH)2
CAS號碼:
分子量::
139.92
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

化驗

≥95%

形狀

solid

mp

101-110 °C (lit.)

SMILES 字串

OB(O)c1ccccc1F

InChI

1S/C6H6BFO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H

InChI 密鑰

QCSLIRFWJPOENV-UHFFFAOYSA-N

應用

用于制备具生物活性的联苯化合物和二氟化芳基硼路易斯酸。
Reactant for:
  • Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes
  • Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation
  • Site-selective Suzuki-Miyaura arylation reactions
  • Rh-catalyzed enantioselective addition reactions
  • Rhodium- and Palladium-catalyzed substitution reactions

其他說明

含不定量的酸酐

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

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析證明 (COA)

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Helvetica Chimica Acta, 78, 2026-2026 (1995)
The Journal of Organic Chemistry, 60, 3020-3020 (1995)
Mikhail Y Vorona et al.
Materials (Basel, Switzerland), 13(8) (2020-04-26)
Anthracene-based semiconductors have attracted great interest due to their molecular planarity, ambient and thermal stability, tunable frontier molecular orbitals and strong intermolecular interactions that can lead to good device field-effect transistor performance. In this study, we report the synthesis of

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