Ferrocenecarboxaldehyde
Ferrocenecarboxaldehyde structure
|
Common Name | Ferrocenecarboxaldehyde | ||
|---|---|---|---|---|
| CAS Number | 12093-10-6 | Molecular Weight | 214.042 | |
| Density | 1.149g/cm3 | Boiling Point | 213.6ºC at 760 mmHg | |
| Molecular Formula | C11H10FeO | Melting Point | 118-120 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 98.8ºC | |
|
Photocytotoxic oxovanadium(IV) complexes of ferrocenyl-terpyridine and acetylacetonate derivatives.
Eur. J. Med. Chem. 92 , 332-41, (2015) Oxovanadium(IV) complexes [VO(Fc-tpy)(acac)](ClO4) (1), [VO(Fc-tpy)(nap-acac)](ClO4) (2), [VO(Fc-tpy)(py-acac)](ClO4) (3) and [VO(Ph-tpy)(py-acac)](ClO4) (4) of 4'-ferrocenyl-2,2':6',2"-terpyridine (Fc-tpy) and 4'-phenyl-2,2':6',2"-terpyridine (Ph-tpy) having... |
|
|
Interaction of ferrocene appended Ru(II), Rh(III) and Ir(III) dipyrrinato complexes with DNA/protein, molecular docking and antitumor activity.
Eur. J. Med. Chem. 84 , 17-29, (2014) Efficacy of the ferrocene appended piano-stool dipyrrinato complexes [(η(6)-C6H6)RuCl(fcdpm)] (1), [(η(6)-C10H14)RuCl(fcdpm)] (2), [(η(6)-C12H18)RuCl(fcdpm)] (3) [(η(5)-C5Me5)RhCl(fcdpm)] (4) and [(η(5)-C5Me5)IrCl(fcdpm)] (5) [fcdpm = 5-ferrocenyldipyrromethe... |
|
|
A carbon nanotube/poly [Ni-(Protoporphyrin IX)] composite for amperometric detection of long chain aliphatic amines.
Bioelectrochemistry 104 , 51-7, (2015) Poly [Ni-Protoporphyrin] film (pNiPP), containing multiwall carbon nanotubes (MWCNT) was used to cover a glassy carbon electrode. The hybrid material (pNiPP/MWCNT) successfully combines the permselectivity of pNiPP with the high conductivity of MWCNT. The mod... |
|
|
New zinc(II)-based catalyst for asymmetric azomethine ylide cycloaddition reactions.
Org. Lett. 8 , 4687, (2006) [reaction: see text] A new chiral aziridino alcohol ligand for zinc(II)-catalyzed azomethine ylide cycloadditions is described. In the presence of this catalyst, N-arylidene glycine methyl esters react with a variety of dipolarophiles to give substituted pyrr... |
|
|
Antileishmanial activity of quinazoline derivatives: synthesis, docking screens, molecular dynamic simulations and electrochemical studies.
Eur. J. Med. Chem. 92C , 314-331, (2014) A series of quinazoline-2,4,6-triamine were synthesized and evaluated in vitro against Leishmania mexicana. Among them, N(6)-(ferrocenmethyl)quinazolin-2,4,6-triamine (H2) showed activity on promastigotes and intracellular amastigotes, as well as low cytotoxi... |
|
|
Structural and biological investigation of ferrocene-substituted 3-methylidene-1,3-dihydro-2H-indol-2-ones.
Dalton Trans. (6) , 918-21, (2009) The Knoevenagel condensation of 1,3-dihydro-2H-indol-2-one with ferrocene carboxaldehyde afforded an approximate 2:1 mixture of the geometrical isomers (E)- and (Z)-3-ferrocenylmethylidene-1,3-dihydro-2H-indol-2-one respectively in an overall 67% yield; the a... |
|
|
Electrochemical probe for on-chip type flow immunoassay: immunoglobulin G labeled with ferrocenecarboaldehyde.
Biotechnol. Bioeng. 90(1) , 14-9, (2005) Labeling of ferrocenecarboaldehyde (Fc-CHO) to immunoglobulin G (IgG) via formation of Schiff-base and its reduction was investigated for construction of an electrochemical probe for miniaturized amperometric flow immunoassay. Approximately eight molecules of... |
|
|
Ferrocenecarboxaldehyde labeled DNA probe for the study on DNA damage and protection.
Fresenius J. Anal. Chem. 367(6) , 593-5, (2000) A ferrocenecarboxaldehyde (FCA) labeled DNA probe is used for the first time in the study of DNA damage and protection. The electrochemically active reagent FCA was labeled successfully on to a denatured calf-thymus DNA by 1-ethyl-3- (3-dimethyl-aminopropyl) ... |
|
|
Preparation and redox-controlled reversible response of ferrocene-modified poly(allylamine hydrochloride) microcapsules.
Langmuir 27(4) , 1286-91, (2011) Single-component microcapsules were fabricated by the in situ reaction of ferrocenecarboxaldehyde (Fc-CHO) with poly(allylamine hydrochloride) (PAH) doped inside CaCO(3) microparticles, followed by core removal. The PAH-Fc microcapsules had very thick shells ... |
|
|
Kubab, N., et al.
Analusis 17 , 559-564, (1989)
|