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Merck

593060

Sigma-Aldrich

2,6-二氟-4-甲氧基苯硼酸

≥95%

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About This Item

经验公式(希尔记法):
C7H7BF2O3
分子量:
187.94
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

125-130 °C (lit.)

SMILES 字串

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

InChI

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

InChI 密鑰

WVSZSFADEBGONQ-UHFFFAOYSA-N

應用

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

其他說明

含有不定量的酸酐

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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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