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经验公式(希尔记法):
C25H33P
化学文摘社编号:
分子量:
364.50
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22
MDL number:
产品名称
2-二环己基磷-2′-甲基联苯, 97%
SMILES string
Cc1ccccc1-c2ccccc2P(C3CCCCC3)C4CCCCC4
InChI
1S/C25H33P/c1-20-12-8-9-17-23(20)24-18-10-11-19-25(24)26(21-13-4-2-5-14-21)22-15-6-3-7-16-22/h8-12,17-19,21-22H,2-7,13-16H2,1H3
InChI key
GPVWUKXZFDHGMZ-UHFFFAOYSA-N
assay
97%
form
solid
reaction suitability
reagent type: ligand
reaction type: Arylations, reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction, reagent type: ligand
reaction type: Suzuki-Miyaura Coupling
mp
105-109 °C
functional group
phosphine
Quality Level
Application
Legal Information
用法以美国专利 6307087 和 6395916 为准。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
David S Surry et al.
Angewandte Chemie (International ed. in English), 47(34), 6338-6361 (2008-07-30)
Palladium-catalyzed amination reactions of aryl halides have undergone rapid development in the last 12 years, largely driven by the implementation of new classes of ligands. Biaryl phosphanes have proven to provide especially active catalysts in this context. This Review discusses
David S Surry et al.
Chemical science, 2(1), 27-50 (2011-01-01)
Dialkylbiaryl phosphines are a valuable class of ligand for Pd-catalyzed amination reactions and have been applied in a range of contexts. This review attempts to aid the reader in the selection of the best choice of reaction conditions and ligand
Ruben Martin et al.
Accounts of chemical research, 41(11), 1461-1473 (2008-07-16)
The cores of many types of polymers, ligands, natural products, and pharmaceuticals contain biaryl or substituted aromatic structures, and efficient methods of synthesizing these structures are crucial to the work of a broad spectrum of organic chemists. Recently, Pd-catalyzed carbon-carbon
商品
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
相关内容
Phosphine Ligand Application Guide
Buchwald Portfolio: Palladacycles and Ligands
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