471933
4-碘苯硼酸
≥95.0%
别名:
B-(4-iodophenyl)-boronic acid, p-Iodophenylboronic acid, p-iodo-benzeneboronic acid
质量水平
方案
≥95.0%
mp
326-330 °C (lit.)
官能团
iodo
SMILES字符串
OB(O)c1ccc(I)cc1
InChI
1S/C6H6BIO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI key
PELJYVULHLKXFF-UHFFFAOYSA-N
应用
试剂用于
试剂用于制备
- 铜介导的无配体好氧氟烷基化
- 钯催化的好氧氧化交叉偶联反应
- 用于 Suzuki 偶联反应的可回收磁性纳米离子负载的钯催化剂
- 使用铜（Cu）催化剂的氧化羟基化
- 无配体钯催化的 Suzuki-Miyaura 交叉偶联
- 使用金盐催化剂的同型偶联
- 钌（Ru）催化的交叉偶联
- CuI 催化的 Suzuki 偶联反应
- 钯催化的多米诺骨牌 Heck-Mizoroki/Suzuki-Miyaura 反应
- 三乙酸锰介导的芳基硼酸向烯烃的自由基加成
试剂用于制备
- 通过“点击化学”策略合成截短侧耳素衍生物，进行用于研究与核糖体结合和抗菌活性
- 液晶聚乙炔衍生物
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
储存分类代码
11 - Combustible Solids
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
Disubstituted Liquid Crystalline Polyacetylene Derivatives That Exhibit Linearly Polarized Blue and Green Emissions
San Jose, B. A.; et al.
Macromolecules, 44, 6288-6302 (2011)
B M Kinsey et al.
Nuclear medicine and biology, 20(1), 13-22 (1993-01-01)
Three iodinated phenylboronic acids have been synthesized: 4-iodophenylboronic acid (2a), 3-(4-iodobenzenesulfonamido)phenylboronic acid (5a) and 3-(5-dimethylamino-6-iodo-1-naphthalenesulfonamido)phenylboronic acid (6a). The corresponding no-carrier-added 125I derivatives 2b, 5b and 6b have been prepared in good yield by selective displacement of the tributylstannyl group. Compound
Alison M Berezuk et al.
Scientific reports, 8(1), 12933-12933 (2018-08-30)
In Escherichia coli, formation of new cells is mediated by the elongasome and divisome that govern cell elongation and septation, respectively. Proper transition between these events is essential to ensure viable progeny are produced; however, the components of each complex
CuI-catalyzed Suzuki coupling reaction of organoboronic acids with alkynyl bromides
S. Wang, et al.,
Tetrahedron, 67, 4800-4806 (2011)
Kiyofumi Inamoto et al.
Chemical communications (Cambridge, England), 47(42), 11775-11777 (2011-10-01)
Copper-catalysed oxidative hydroxylation of arylboronic acids was accomplished in water containing an amphiphilic surfactant, providing facile access to phenol derivatives.
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