推荐产品
品質等級
化驗
≥95%
mp
163-166 °C (lit.)
官能基
fluoro
SMILES 字串
OB(O)c1cccc(c1)C(F)(F)F
InChI
1S/C7H6BF3O2/c9-7(10,11)5-2-1-3-6(4-5)8(12)13/h1-4,12-13H
InChI 密鑰
WOAORAPRPVIATR-UHFFFAOYSA-N
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應用
作为反应物，参与以下反应：
- Suzuki-Miyaura交叉偶联反应
- 氧气条件下的氧化交叉偶联反应
- 微波辅助的Petasis反应
- 铑催化的加成反应
- 生物活性分子合成反应
其他說明
含有不定量的酸酐。
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)
其他客户在看
Anna Minkkilä et al.
Journal of medicinal chemistry, 51(22), 7057-7060 (2008-11-06)
A series of commercial phenyl-, heteroaryl-, alkyl-, and alkenylboronic acids were evaluated for their FAAH and MGL inhibitory activities. The compounds were generally selective for FAAH, with IC50 in the nanomolar or low-micromolar range. Eight of these compounds inhibited MGL
Gözde Murat Saltan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 188, 372-381 (2017-08-02)
In an approach to develop efficient organic optoelectronic devices to be used in light-driven systems, a series of three thiophene linked benzimidazole conjugates were synthesized and characterized. The combination of two thiophene rings to a benzimidazole core decorated with different
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