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Merck
CN

593060

2,6-二氟-4-甲氧基苯硼酸

≥95%

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经验公式(希尔记法):
C7H7BF2O3
化学文摘社编号:
分子量:
187.94
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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InChI

1S/C7H7BF2O3/c1-13-4-2-5(9)7(8(11)12)6(10)3-4/h2-3,11-12H,1H3

SMILES string

COc1cc(F)c(B(O)O)c(F)c1

InChI key

WVSZSFADEBGONQ-UHFFFAOYSA-N

assay

≥95%

form

solid

mp

125-130 °C (lit.)

functional group

fluoro

Application

2,6-Difluoro-4-methoxyphenylboronic acid can be used:
  • To prepare a ligand N4Py2Ar2, which in turn is used to synthesize a Fe complex, employed in aromatic C−F hydroxylation reactions.
  • As a substrate in the study of copper-catalyzed trifluoromethylthiolation of boronic acids.
  • As a substrate in the preparation of a thio xylopyranoside as a potent antithrombotic agent.

Reactant involved in Suzuki and Stille coupling reactions for synthesis of antithrombotic drugs

Other Notes

含有不定量的酸酐

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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Aromatic C-F Hydroxylation by Nonheme Iron (IV)-Oxo Complexes: Structural, Spectroscopic, and Mechanistic Investigations
Sahu S, et al.
Journal of the American Chemical Society, 138(39), 12791-12802 (2016)
Mild and soft catalyzed trifluoromethylthiolation of boronic acids: the crucial role of water
Glenadel Q, et al.
Chemistry?A European Journal , 21(42), 14694-14698 (2015)
Palladium-catalyzed C-C coupling: efficient preparation of new 5-thio-beta-d-xylopyranosides as oral venous antithrombotic drugs
Bondoux M, et al.
Tetrahedron Letters, 50(27), 3872-3876 (2009)

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