推荐产品
质量水平
方案
97%
表单
solid
反应适用性
reagent type: ligand
reaction type: Baeyer-Villiger Oxidation
reagent type: ligand
reaction type: Cycloadditions
reagent type: ligand
reaction type: Reductions
mp
183-188 °C (lit.)
官能团
phosphine
SMILES字符串
c1ccc(cc1)P(c2ccccc2)c3ccccc3P(c4ccccc4)c5ccccc5
InChI
1S/C30H24P2/c1-5-15-25(16-6-1)31(26-17-7-2-8-18-26)29-23-13-14-24-30(29)32(27-19-9-3-10-20-27)28-21-11-4-12-22-28/h1-24H
InChI key
NFRYVRNCDXULEX-UHFFFAOYSA-N
应用
1,2-双(二苯基膦基)苯(DPPB)可用于:
- 作为螯合配体,用于合成发光铜(I)卤化物配合物。
- 合成铜-1,2-双(二苯基膦基)苯催化剂,该催化剂用于 β-硼化 α, β-不饱和酰胺。
- 作为TMEDA的替代品,在铁催化的氟代芳族偶联反应中,选择性断裂 sp3 C-X键。
- 作为配体,从炔类酯合成烯基硼酸酯。
- 合成铜-二膦配合物,用作多种胺的 N-甲酰化的均相催化剂。
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
Eyeshields, Gloves, type N95 (US)
Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1, 2-bis (diphenylphosphino) benzene
Hatakeyama T, et al.
Chemical Communications (Cambridge, England), 351(10), 1216-1218 (2009)
Copper-Catalyzed Conjugate Addition of Diboron Reagents to α, β -Unsaturated Amides: Highly Reactive Copper-1, 2-Bis (diphenylphosphino) benzene Catalyst System
Chea H, et al.
advanced synthesis and catalysis, 351(6), 855-858 (2009)
Photophysical properties of highly luminescent copper (I) halide complexes chelated with 1, 2-bis (diphenylphosphino) benzene
Tsuboyama A, et al.
Inorganic Chemistry, 46(6), 1992-2001 (2007)
Copper-Catalyzed Conjugate Addition of Diboron Reagents to α, β -Unsaturated Amides: Highly Reactive Copper-1, 2-Bis (diphenylphosphino) benzene Catalyst System
Chea H, et al.
Advanced Synthesis & Catalysis, 351(6), 855-858 (2009)
Copper-diphosphine complex catalysts for N-formylation of amines under 1 atm of carbon dioxide with polymethylhydrosiloxane
Motokura K, et al.
Catalysis Science & Technology, 3(9), 2392-2396 (2013)
商品
Baeyer-Villiger氧化是与羰基相邻的碳-碳键的氧化裂解,其可将酮转化为酯、环酮转化为内酯。
The Baeyer-Villiger oxidation is the oxidative cleavage of a carbon-carbon bond adjacent to a carbonyl, which converts the ketones to esters and the cyclic ketones to lactones.
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