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质量水平
检测方案
97%
mp
256-263 °C (lit.)
SMILES字符串
Cc1ccc(cc1)B(O)O
InChI
1S/C7H9BO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5,9-10H,1H3
InChI key
BIWQNIMLAISTBV-UHFFFAOYSA-N
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应用
试剂用于
制备过程中使用的试剂
- 钯 (Pd) 催化的直接芳基化
- 直接钯 (II) 催化合成
- 水中 Suzuki-Miyaura 交叉偶联的钯催化芳基化
- 环钯化反应
- 串联型钯 (II) 催化的氧化 Heck 反应和分子内 C-H 酰胺化反应
- 钌催化直接芳基化
- 铑催化不对称共轭加成
- 无配体铜催化的交叉偶联反应
- Suzuki-Miyaura 和 Sonogashira 交叉偶联反应的区域选择性芳基化和炔基化
- 无配体 Suzuki、Sonogashira 和 Heck 交叉偶联反应
制备过程中使用的试剂
- 溴代芳烃的 Suzuki-Miyaura 交叉偶联反应的催化剂
- 通过点击离子共聚物固定的,用于 Suzuki-Miyaura 在水中的交叉偶联反应的可再循环的钯纳米颗粒催化剂
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
ACS Symp. Ser., 642, 194-205 (1996)
Palladium nanoparticles immobilized by click ionic copolymers: Efficient and recyclable catalysts for Suzuki-Miyaura cross-coupling reaction in water
Catalysis Communications, 22, 83-88 (2012)
Biomaterials, 178, 608-619 (2018-04-02)
Inflammation serves as a natural defense mechanism to protect living organisms from infectious diseases. Nonsteroidal anti-inflammatory drugs (NSAIDs) can help relieve inflammatory reactions and are clinically used to treat pain, fever, and inflammation, whereas long-term use of NSAIDs may lead
Carbon-Carbon Bond Formation by Ligand-free Cross-Coupling Reaction Using Palladium Catalyst Supported on Synthetic Adsorbent
ChemCatChem, 4, 546-558 (2012)
Organic letters, 14(9), 2394-2397 (2012-04-19)
A fast and convenient synthesis of arylamidines starting from readily available potassium aryltrifluoroborates and cyanamides is reported. The coupling was achieved by Pd(II)-catalysis in a one step 20 min microwave protocol using Pd(O(2)CCF(3)), 6-methyl-2,2'-bipyridyl, TFA, and MeOH, providing the corresponding
商品
MIDA-protected boronate esters offer stability, chromatography compatibility, and reactivity in anhydrous cross-coupling conditions.
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