推荐产品
方案
≥98%
反应适用性
core: iron
reagent type: catalyst
mp
105-107 °C (lit.)
SMILES字符串
[Fe].[CH]1[CH][CH][CH][CH]1.O=C([C]2[CH][CH][CH][CH]2)c3ccccc3
InChI
1S/C12H9O.C5H5.Fe/c13-12(11-8-4-5-9-11)10-6-2-1-3-7-10;1-2-4-5-3-1;/h1-9H;1-5H;
InChI key
JJHHJZCYDPLHIL-UHFFFAOYSA-N
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应用
Reactant for:
Reactant for synthesis of:
- Deprotonative metalation of ferrocenes
- Oxidative chemistry
- Reduction of ferrocenyl ketones
- Polymerization of C-ferrocenyl-substituted phosphaalkene
Reactant for synthesis of:
- Planat chiral triferrocenylmethane derivative
- Chiral ferrocenyl alcohols via asymmetric transfer hydrogenation
储存分类代码
13 - Non 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)
Yong Leng Kelvin Tan et al.
Dalton transactions (Cambridge, England : 2003), 48(48), 10871-10881 (2009-12-22)
A series of compounds is described in which one of the ethyl groups in diethylstilbestrol has been replaced by a ferrocenyl substituent. Only those derivatives incorporating phenol moieties underwent isomerisation from the Z to the E form, and some of
Gandrath Dayaker et al.
Chemical communications (Cambridge, England), 46(16), 2862-2864 (2010-04-07)
A mixed lithium-cadmium amide and a combination of lithium and zinc amides were reacted with a range of ferrocenes; deprotonative mono- or dimetallation in general occurred chemoselectively at room temperature, as evidenced by subsequent quenching with iodine.
H. Zhang and Z. Bian,
Journal of Organometallic Chemistry, 692, 5687-5689 (2007)
Y. Wu, et al.,
Tetrahedron Asymmetry, 20, 584-587 (2009)
J. R. Garabatos-Perera and H. Butenschoen,
Journal of Organometallic Chemistry, 694, 2047-2052 (2009)
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