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335061

Sigma-Aldrich

Ferrocenemethanol

97%

Synonym(s):

FcMeOH, (Hydroxymethyl)ferrocene, Ferrocenylcarbinol

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500 MG
HUF 33,700.00
5 G
HUF 116,000.00

About This Item

Empirical Formula (Hill Notation):
C11H12FeO
CAS Number:
1273-86-5
Molecular Weight:
216.06
MDL number:
MFCD00040878
UNSPSC Code:
12161600
PubChem Substance ID:
24860285
NACRES:
NA.22

HUF 33,700.00

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Quality Level

200

Assay

97%

form

solid

reaction suitability

core: iron
reagent type: catalyst

mp

79-81 °C (lit.)

SMILES string

[Fe].[CH]1[CH][CH][CH][CH]1.OC[C]2[CH][CH][CH][CH]2

InChI

1S/C6H7O.C5H5.Fe/c7-5-6-3-1-2-4-6;1-2-4-5-3-1;/h1-4,7H,5H2;1-5H;

InChI key

QETISSZVCNFQBN-UHFFFAOYSA-N

Related Categories

Application

  • Ferrocenemethanol (FcMeOH) is commonly used as a water soluble ferrocene based reference redox system in electrochemical studies.[1][2]
  • It is used in the synthesis of ferrocenylmethoxy-isatins, potent antiproliferative agents.[3]
  • FcMeOH can be employed in the preparation of ferrocene-carbohydrate conjugates for biosensing applications.[4]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000332064
0000353242
0000332063
0000318086
0000318086

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Effect of the mediator in feedback mode-based SECM interrogation of indium tin-oxide and boron-doped diamond electrodes.
Neufeld A K and O?Mullane A P
Journal of Solid State Electrochemistry, 10(10), 808-816 (2006)
Jingyi Wang et al.
Journal of colloid and interface science, 570, 350-361 (2020-03-18)
Molybdenite (MoS2) has attracted great attention in the field of advanced materials. MoS2 is normally separated from other minerals by selective flotation, and chemical reagents (so-called depressants) are required to lower the surface hydrophobicity of MoS2. Previous studies had controversial
Azide?Alkyne Cycloaddition En Route to 1 H-1, 2, 3-Triazole-Tethered Isatin?Ferrocene, Ferrocenylmethoxy?Isatin, and Isatin?Ferrocenylchalcone Conjugates: Synthesis and Antiproliferative Evaluation.
Singh A, et al.
ACS Omega, 3(1), 1263-1268 (2018)
Convenient methods for the synthesis of ferrocene? carbohydrate conjugates.
Casas-Solvas J M, et al.
Organic Letters, 6(21), 3687-3690 (2004)
Anthony P O'Mullane et al.
Analytical chemistry, 80(12), 4614-4626 (2008-05-20)
An analytical evaluation of the higher ac harmonic components derived from large amplitude Fourier transformed voltammetry is provided for the reversible oxidation of ferrocenemethanol (FcMeOH) and oxidation of uric acid by an EEC mechanism in a pH 7.4 phosphate buffer
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