593060
2,6-Difluoro-4-methoxyphenylboronic acid
≥95%
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About This Item
Empirical Formula (Hill Notation):
C7H7BF2O3
CAS Number:
Molecular Weight:
187.94
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Product Name
2,6-Difluoro-4-methoxyphenylboronic acid, ≥95%
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
Contains varying amounts of anhydride
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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)
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)
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)
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