349585
Benzoylferrocene
≥98%
동의어(들):
Ferrecenophenone, Ferrocenyl phenyl ketone, Ferrocenyl(phenyl)methanone, NSC 54800, (Benzoylcyclopentadienyl)cyclopentadienyliron
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C17H14FeO
CAS Number:
Molecular Weight:
290.14
EC Number:
MDL number:
UNSPSC 코드:
12352300
PubChem Substance ID:
NACRES:
NA.22
추천 제품
![Sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate](/deepweb/assets/sigmaaldrich/product/structures/251/439/7a621e74-bfd1-4a43-833c-09adfcc1e0b3/640/7a621e74-bfd1-4a43-833c-09adfcc1e0b3.png)
분석
≥98%
반응 적합성
core: iron
reagent type: catalyst
mp
105-107 °C (lit.)
SMILES string
[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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애플리케이션
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
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
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A series of compounds is described in which one of the ethyl groups in diethylstilbestrol has been replaced by a ferrocenyl substituent.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
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.
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)
H. Zhang and Z. Bian,
Journal of Organometallic Chemistry, 692, 5687-5689 (2007)
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