335061
Ferrocenemethanol
97%
Sinônimo(s):
FcMeOH, (Hydroxymethyl)ferrocene, Ferrocenylcarbinol
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About This Item
Fórmula empírica (Notação de Hill):
C11H12FeO
Número CAS:
Peso molecular:
216.06
Número MDL:
Código UNSPSC:
12161600
ID de substância PubChem:
NACRES:
NA.22
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Ensaio
97%
Formulário
solid
adequação da reação
core: iron
reagent type: catalyst
pf
79-81 °C (lit.)
cadeia de caracteres SMILES
[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;
chave InChI
QETISSZVCNFQBN-UHFFFAOYSA-N
Categorias relacionadas
Aplicação
- Ferrocenemethanol (FcMeOH) is commonly used as a water soluble ferrocene based reference redox system in electrochemical studies.
- It is used in the synthesis of ferrocenylmethoxy-isatins, potent antiproliferative agents.
- FcMeOH can be employed in the preparation of ferrocene-carbohydrate conjugates for biosensing applications.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Convenient methods for the synthesis of ferrocene? carbohydrate conjugates.
Casas-Solvas J M, et al.
Organic Letters, 6(21), 3687-3690 (2004)
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)
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Neufeld A K and O?Mullane A P
Journal of Solid State Electrochemistry, 10(10), 808-816 (2006)
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