推荐产品
质量水平
检测方案
97%
形式
solid
反应适用性
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
reaction type: Cross Couplings
pH值（酸碱度）
1.79 (1% in solution)
mp
>230 °C (lit.)
官能团
phosphine
SMILES字符串
F[B-](F)(F)F.C[PH+](C(C)(C)C)C(C)(C)C
InChI
1S/C9H21P.BF4/c1-8(2,3)10(7)9(4,5)6;2-1(3,4)5/h1-7H3;/q;-1/p+1
InChI key
BRDLRXCAHKUWJS-UHFFFAOYSA-O
正在寻找类似产品? 访问 产品对比指南
应用
二-叔-丁基（甲基）膦四氟硼酸盐可用于制备带有 C4 苯基取代基的对嘌呤类似物的前体，该前体对 5-HT2B 受体具有亲和性。它也可以用于钯催化的伯烷基亲电子试剂（溴化物、碘化物或甲苯磺酸盐）的硼化反应中，使用联硼酸频那醇酯或联硼酸新戊二醇酯作为硼源。
鏻盐可用于 Pd 催化的交叉偶联反应。
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Palladium-catalyzed borylation of primary alkyl bromides.
Joshi-Pangu A, et al.
The Journal of Organic Chemistry, 77(15), 6629-6633 (2012)
Jian-Xin Wang et al.
Organic letters, 10(14), 2923-2926 (2008-06-26)
A general and efficient synthesis of 5-aryl imidazo[1,5- a]pyrazines by palladium-catalyzed coupling of the corresponding 8-substituted derivatives with aryl halides is described. The scope of this new reaction for the imidazo[1,5- a]pyrazine ring system was explored using three readily available
Marc Lafrance et al.
Journal of the American Chemical Society, 128(27), 8754-8756 (2006-07-06)
Penta-, tetra-, tri-, and difluorobenzenes undergo direct arylation with a wide range of arylhalides in high yield. Inverse reactivity is observed compared to the common electrophilic aromatic substitution pathway since electron-deficient, C-H acidic arenes react preferentially. Computational studies indicate that
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