物质信息
ID:355862
名称和标识
IUPAC传统名
di-tert-butyl(2-phenylphenyl)phosphane
IUPAC标准名
di-tert-butyl(2-phenylphenyl)phosphane
别名
2-(二-叔-丁基膦基)联苯(2-Biphenyl)di-tert-butylphosphine2-(二叔丁基膦)联苯(2-Biphenylyl)di-tert-butylphosphineJohnPhos2-(Di-tert-butylphosphino)biphenyl(2-联苯基)二-叔丁基膦
化合物性质
理化性质
熔点
86-88 °C(lit.)
产品相关信息
纯度
≥97.0% (GC)
线性分子式
C6H5C6H4P[C(CH3)3]2
级别
purum
安全信息
MSDS下载
德国WGK号
3
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
GHS危险声明
H413
描述信息
Other Notes
新型胺化反应（Buchwald 反应）的最佳配体1
Application
Ligand utilized in amination of aryl halides and aryl triflates.1Catalyst for:
• Decarboxylative cross-coupling of dialkoxybenzoic acids with diaryl disulfides or diaryl diselenides2
• Stereoselective preparation of imidazolidinones via intramolecular hydroamination of N-allylic-N-arylureas3
• Regioselective arylation of olefins with aryl chlorides4
• Cross-coupling reaction for the synthesis of polyunsaturated macrolactones5
• Regioselective O-alkylation reactions6
• Sonogashira-type cross coupling7
新型胺化反应（Buchwald 反应）的最佳配体1
Application
Ligand utilized in amination of aryl halides and aryl triflates.1Catalyst for:
• Decarboxylative cross-coupling of dialkoxybenzoic acids with diaryl disulfides or diaryl diselenides2
• Stereoselective preparation of imidazolidinones via intramolecular hydroamination of N-allylic-N-arylureas3
• Regioselective arylation of olefins with aryl chlorides4
• Cross-coupling reaction for the synthesis of polyunsaturated macrolactones5
• Regioselective O-alkylation reactions6
• Sonogashira-type cross coupling7
分子图谱
暂无数据
点击上传数据
参考文献
暂无数据
点击上传数据