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关于此项目
经验公式(希尔记法):
C24H23FeP
化学文摘社编号:
分子量:
398.26
UNSPSC Code:
12352300
PubChem Substance ID:
MDL number:
InChI
1S/C19H18P.C5H5.Fe/c1-16(17-10-8-9-11-17)20(18-12-4-2-5-13-18)19-14-6-3-7-15-19;1-2-4-5-3-1;/h2-16H,1H3;1-5H;
SMILES string
[Fe].[CH]1[CH][CH][CH][CH]1.CC([C]2[CH][CH][CH][CH]2)P(c3ccccc3)c4ccccc4
InChI key
WNHZFUIMWGWGNB-UHFFFAOYSA-N
form
solid
reaction suitability
core: palladium, 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: catalyst
reaction type: Coupling Reactions
signalword
Warning
hcodes
Hazard Classifications
Repr. 2 - Skin Irrit. 2
存储类别
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Ping He et al.
Organic letters, 9(2), 343-346 (2007-01-16)
Anionic four-electron donor-based palladacycle-catalyzed 1,4-additions of arylboronic acids with alpha,beta-unsaturated ketones and 1,2-additions of arylboronic acids with aldehydes and alpha-ketoesters are described. Our study demonstrated that palladacycles were highly efficient, practical catalysts for these addition reactions. The work described here
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