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化驗
≥98%
反應適用性
core: iron
reagent type: catalyst
mp
105-107 °C (lit.)
SMILES 字串
[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 密鑰
JJHHJZCYDPLHIL-UHFFFAOYSA-N
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應用
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
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
客戶也查看了
Kevin J T Noonan et al.
Chemical communications (Cambridge, England), 35(35), 3658-3660 (2007-08-31)
The addition polymerization of a ferrocenyl-substituted P[double bond]C bond leads to new redox-active polymers with functional ferrocene and phosphine moieties.
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A series of compounds is described in which one of the ethyl groups in diethylstilbestrol has been replaced by a ferrocenyl substituent.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.
J. R. Garabatos-Perera and H. Butenschoen,
Journal of Organometallic Chemistry, 694, 2047-2052 (2009)
Y. Wu, et al.,
Tetrahedron Asymmetry, 20, 584-587 (2009)
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