所有图片(3)
别名:
4-氟苯硼酸, NSC 142683
线性分子式:
FC6H4B(OH)2
CAS号:
分子量:
139.92
Beilstein:
2829653
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
检测方案
≥95%
形式
powder
mp
262-265 °C (lit.)
SMILES字符串
OB(O)c1ccc(F)cc1
InChI
1S/C6H6BFO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI key
LBUNNMJLXWQQBY-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
4-氟基苯硼酸可用作反应物，参与四氟硼酸芳香重氮盐、 碘鎓盐和碘烷的偶联反应。它还被用于生产具有生物活性的新型三联苯。
它也可作为反应物参与：
它也可作为反应物参与：
- 使用微波和triton B催化剂的Suzuki偶联。
- Pd催化的吡唑与苯硼酸的直接芳基化反应。
- 钯纳米粒子催化的 Mizoroki-Heck 和 Suzuki-Miyaura 偶联反应。
- Cu催化的Petasis反应。
- 串联型Pd(II)催化的氧化Heck反应和分子内C-H酰胺化序列。
- 钌催化的直接芳基化。
- Rh催化的不对称耦合物加合。
- 无配体铜催化的硝基芳烃与芳基硼酸的偶联。
- 通过Suzuki-Miyaura和Sonogashira交叉偶联反应进行区域选择性芳基化和炔基化。
- 四溴噻吩的Suzuki交叉偶联。
- 腈的钯催化加成。
其他说明
含不定量的酸酐
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Yuvraj Satkar et al.
Frontiers in chemistry, 8, 563470-563470 (2020-11-17)
The chemoselective reaction of the C- followed by the O-centered naphthyl radicals with the more electron-deficient hypervalent bond of the diaryliodonium(III) salts is described. This discovered reactivity constitutes a new activation mode of the diaryliodonium(III) salts which enabled a one-pot
Suk-Ku Kang et al.
The Journal of organic chemistry, 61(14), 4720-4724 (1996-07-12)
The palladium-catalyzed cross-coupling reaction of iodinanes (iodonium salts and iodanes) with organoboron compounds to form carbon-carbon bonds was achieved at ambient temperature under aqueous conditions in the absence of base. Coupling of phenylboronic acid with diphenyliodonium tetrafluoroborate in the presence
J J Li et al.
Journal of medicinal chemistry, 39(9), 1846-1856 (1996-04-26)
A novel series of terphenyl methyl sulfones and sulfonamides have been shown to be highly potent and selective cyclooxygenase-2 (COX-2) inhibitors. The sulfonamide analogs 17 and 21 were found to be much more potent COX-2 inhibitors and orally active anti-inflammatory
Robin Frauenlob et al.
The Journal of organic chemistry, 77(9), 4445-4449 (2012-04-13)
We have developed a copper-catalyzed process for the coupling of aldehydes, amines, and boronic acids. This allows greater reactivity with simple aryl boronic acids and allows coupling reactions to proceed that previously failed. Initial mechanistic studies support a process involving
Microwave-enhanced triton B catalyzed Suzuki coupling reaction
Meshram, H. M.; et al.
Indian J. Chem. B, 51, 362-365 (2012)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门