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122459

Ferrocenecarboxaldehyde

Name: Ferrocenecarboxaldehyde
Brand: ALDRICH

98%, solid

Synonym(s):

Cyclopentadienyl(formylcyclopentadienyl)iron

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About This Item

Empirical Formula (Hill Notation):

C₁₁H₁₀FeO

CAS Number:

12093-10-6

Molecular Weight:

214.04

NACRES:

NA.22

PubChem Substance ID:

24847489

UNSPSC Code:

12352300

EC Number:

235-158-1

MDL number:

MFCD00001429

Assay:

98%

Form:

solid

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Properties

Product Name

Ferrocenecarboxaldehyde, 98%

Quality Level

100

assay

98%

form

solid

reaction suitability

core: iron, reagent type: catalyst

mp

118-120 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

SMILES string

[Fe].[CH]1[CH][CH][CH][CH]1.[H]C(=O)[C]2[CH][CH][CH][CH]2

InChI

1S/C6H5O.C5H5.Fe/c7-5-6-3-1-2-4-6;1-2-4-5-3-1;/h1-5H;1-5H;

InChI key

UQTCQJVPLIVCAX-UHFFFAOYSA-N

Description

Application

Used to prepare chiral ferrocene aziridinylmethanols for selective azomethine ylide cycloaddtion.

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Preparation and redox-controlled reversible response of ferrocene-modified poly(allylamine hydrochloride) microcapsules.

Zhipeng Wang et al.

Langmuir : the ACS journal of surfaces and colloids, 27(4), 1286-1291 (2010-11-04)

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 with remnant PAH-Fc inside, leading to a robust capsule

Structural and biological investigation of ferrocene-substituted 3-methylidene-1,3-dihydro-2H-indol-2-ones.

John Spencer et al.

Dalton transactions (Cambridge, England : 2003), (6)(6), 918-921 (2009-01-29)

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 air and solution-stable isomers were readily separated by preparative thin layer chromatography and

Antileishmanial activity of quinazoline derivatives: synthesis, docking screens, molecular dynamic simulations and electrochemical studies.

Cesar Mendoza-Martínez et al.

European journal of medicinal chemistry, 92, 314-331 (2015-01-13)

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 cytotoxicity in mammalian cells. Docking and electrochemical studies showed the importance of both

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Global Trade Item Number

SKU	GTIN
122459-5G	04061838721259
122459-25G	04061838721242